monarch-initiative/mondo: v2026-05-05

Nicole Vasilevsky; Chris Mungall; Nico Matentzoglu; Sabrina Toro; Trish Whetzel; MeeSiing Ngu; katiermullen; Harshad; Yousif; kallia-p; Lauren; Shahim Essaid; bbopjenkins; Joe Flack; Dragon-AI Agent; actions-user; Patrick Golden; Daniel-Olson; Emily Hartley; Ray Stefancsik; Eric Douglass; Daniel Himmelstein; Charles Tapley Hoyt; Deepak; Jim Balhoff; Kevin Schaper; PaulaDuekRoggli

doi:10.5281/zenodo.20040112

Published May 5, 2026 | Version v2026-05-05

Software Open

monarch-initiative/mondo: v2026-05-05

1. Critical Path Institute
2. Lawrence Berkeley National Laboratory
3. semanticly.ai
4. @monarch-initiative
5. @jhu-bids
6. Monarch Initiative
7. @actions
8. UNC Chapel Hill
9. @radoverlay
10. RWTH Aachen University
11. SIB Swiss Institute of Bioinformatics
12. @RENCI

<details> <summary>Classes added: 1283</summary>

| Term | ----| | sex chromosome difference of sexual development, alpaca (MONDO:7770342) | | cervical incompetence, non-human animal (MONDO:1013409) | | heart defect with mitral regurgitation, saddlebill stork (MONDO:7770422) | | cholesteryl ester storage disease, dog (MONDO:7770652) | | XX difference of sexual development, eastern gray kangaroo (MONDO:7770645) | | folliculitis, non-human animal (MONDO:1013762) | | leukocyte adhesion deficiency, water buffalo (MONDO:7770060) | | diabetic ketoacidosis, non-human animal (MONDO:1013045) | | macrostomus, rabbit (MONDO:7770746) | | quantitative variation vertebrae, medaka (MONDO:7770713) | | leg defects, zebu cattle (MONDO:7770311) | | paraneoplastic syndrome, non-human animal (MONDO:1013179) | | iron deficiency anemia, non-human animal (MONDO:1013084) | | lipoma, non-human animal (MONDO:1013717) | | Luo-Agrawal neurodevelopmental syndrome (MONDO:0981165) | | bone inflammation disease, non-human animal (MONDO:1013778) | | hemochromatosis, dog (MONDO:7770561) | | osteogenesis imperfecta, COL1A1-related, sheep (MONDO:7770697) | | hypertensive retinopathy, non-human animal (MONDO:1013206) | | neuroma, non-human animal (MONDO:1013708) | | lymphangitis, non-human animal (MONDO:1013656) | | enthesopathy, non-human animal (MONDO:1013742) | | caruncular trichiasis, dog (MONDO:7770409) | | carcinoma in situ of urethra, non-human animal (MONDO:1013298) | | biliary atresia, non-human animal (MONDO:1013408) | | ectodermal dysplasia, rabbit (MONDO:7770105) | | haplotype with homozygous deficiency, MTRDHH2 to 5, sheep (MONDO:7770470) | | hypomyelinating polyneuropathy, MPZ-related, dog (MONDO:7770276) | | Chandler syndrome, non-human animal (MONDO:1013035) | | bronchitis, non-human animal (MONDO:1013756) | | anterior ischemic optic neuropathy, non-human animal (MONDO:1013421) | | hyperuricemia, chicken (MONDO:7770441) | | chorioretinitis, non-human animal (MONDO:1013565) | | male subfertility, pig (MONDO:7770443) | | glycogen storage disease VII, non-human animal (MONDO:1013255) | | XX sex reversal, pig (MONDO:7770345) | | spondylolisthesis, chicken (MONDO:7770210) | | small intestine leiomyosarcoma, non-human animal (MONDO:1013354) | | haplotype with homozygous deficiency NH8, cattle (MONDO:7770106) | | amorphus globosus, cattle (MONDO:7770386) | | urethral stricture, non-human animal (MONDO:1013232) | | albinism coat color, red-necked wallaby (MONDO:7770116) | | deficiency color vision, tufted capuchin (MONDO:7770250) | | paraphimosis, non-human animal (MONDO:1013605) | | cutaneous mastocytosis, dog (MONDO:7770414) | | endometritis, non-human animal (MONDO:1013574) | | hantavirus infectious disease, non-human animal (MONDO:1013498) | | polydactyly, SHH-related, domestic cat (MONDO:1013786) | | idiopathic generalized epilepsy, non-human animal (MONDO:1013056) | | cholangitis, non-human animal (MONDO:1013561) | | peptic esophagitis, non-human animal (MONDO:1013167) | | actinic keratosis, non-human animal (MONDO:1013002) | | haplotype with homozygous deficiency, RFC5-related, cattle (MONDO:7770514) | | cystadenocarcinoma, non-human animal (MONDO:1013727) | | paraquat poisoning, non-human animal (MONDO:1013083) | | sebaceous adenoma, non-human animal (MONDO:1013324) | | congenital adrenal hyperplasia, medaka (MONDO:7770604) | | shoulder and hip luxation, cattle (MONDO:7770389) | | tonsillitis, non-human animal (MONDO:1013622) | | paroxysmal dystonia-ataxia syndrome, TNR-related, dog (MONDO:7770208) | | trichomoniasis, non-human animal (MONDO:1013690) | | paw pad hyperkeratosis, GJB6-related, dog (MONDO:7770728) | | neuronal ceroid lipofuscinosis, 3, CLN3-related, cattle (MONDO:7770442) | | photosensitivity disease, non-human animal (MONDO:1013765) | | congenital heart defect, macaque (MONDO:7770637) | | lung neoplasm, non-human animal (MONDO:1013144) | | congenital laryngeal web, non-human animal (MONDO:1013516) | | cytomegalovirus infection, non-human animal (MONDO:1013495) | | short tail sperm, zebu cattle (MONDO:7770358) | | pink eye, chicken (MONDO:7770072) | | corpus callosum hypoplasia / dysplasia, coyote (MONDO:7770506) | | sterile, pig (MONDO:7770214) | | congenital amastia, horse (MONDO:7770271) | | laryngeal carcinoma, non-human animal (MONDO:1013280) | | coccidiosis, non-human animal (MONDO:1013566) | | paroxysmal dyskinesia, PCK2-related, dog (MONDO:7770509) | | pontocerebellar hypoplasia, zebu cattle (MONDO:7770546) | | band keratopathy, non-human animal (MONDO:1013407) | | nasal cavity polyp, non-human animal (MONDO:1013192) | | acute basophilic leukemia, non-human animal (MONDO:1013359) | | precocious puberty, rabbit (MONDO:7770572) | | sciatic neuropathy, non-human animal (MONDO:1013183) | | sterile, male, sheep (MONDO:7770633) | | sinusitis, non-human animal (MONDO:1013750) | | chalazion, non-human animal (MONDO:1013559) | | dental abnormalities, horse (MONDO:7770406) | | external auditory canal atresia, dog (MONDO:7770294) | | seborrheic dermatitis, non-human animal (MONDO:1013042) | | biliary cystadenocarcinoma, non-human animal (MONDO:1013335) | | skin hemangioma, non-human animal (MONDO:1013344) | | cystadenoma, non-human animal (MONDO:1013728) | | rhizomelic chondrodysplasia punctata, cattle (MONDO:7770638) | | coronary artery congenital malformation, non-human animal (MONDO:1013037) | | infertility, dzo (MONDO:7770190) | | urethritis, non-human animal (MONDO:1013624) | | ergotism, non-human animal (MONDO:1013649) | | dens evaginatus, rhesus macaque (MONDO:7770356) | | meningioma, non-human animal (MONDO:1013719) | | cataract, rabbit (MONDO:7770275) | | tricuspid valve disorder, non-human animal (MONDO:1013227) | | intestinal atresia, non-human animal (MONDO:1013419) | | filariasis, non-human animal (MONDO:1013686) | | cholesteatoma of middle ear, non-human animal (MONDO:1013027) | | long QT syndrome, CACNA1C-related, pig (MONDO:7770521) | | chromosomal abnormality, isochromosome, sex chromosome, cattle (MONDO:7770709) | | corpus callosum hypoplasia / dysplasia, dog (MONDO:7770636) | | hiatus hernia, non-human animal (MONDO:1013074) | | nasolacrimal duct obstruction, cattle (MONDO:7770477) | | biliary tract disorder, non-human animal (MONDO:1013385) | | sick sinus syndrome, non-human animal (MONDO:1013209) | | hydrosalpinx, non-human animal (MONDO:1013702) | | angioedema, non-human animal (MONDO:1013671) | | chromosomal structural anomaly, translocation, centric fusion, Eurasian beaver (MONDO:7770675) | | imperforate anus, non-human animal (MONDO:1013012) | | vitamin B12 deficiency, non-human animal (MONDO:1013028) | | acute kidney tubular necrosis, non-human animal (MONDO:1013404) | | Arnold-Chiari malformation, zebu cattle (MONDO:7770508) | | XX difference of sexual development, red kangaroo (MONDO:7770646) | | rectal carcinoma, non-human animal (MONDO:1013278) | | translocation chromosomal structural anomaly, chicken (MONDO:7770660) | | hypervitaminosis A, non-human animal (MONDO:1013499) | | leptospirosis, non-human animal (MONDO:1013587) | | nasal cavity adenocarcinoma, non-human animal (MONDO:1013309) | | mitral valve disorder, non-human animal (MONDO:1013099) | | cardiac malformation, BRI3BP-related, cattle (MONDO:7770557) | | cutaneous myiasis, non-human animal (MONDO:1013431) | | polyploidy, goat (MONDO:7770684) | | sinoatrial block, non-human animal (MONDO:1013448) | | spleen cancer, non-human animal (MONDO:1013152) | | congenital partial colonic agenesis, dog (MONDO:7770352) | | optic neuritis, non-human animal (MONDO:1013168) | | cerebellar ataxia, RALGAPA1-related, dog (MONDO:7770303) | | hepatoblastoma, non-human animal (MONDO:1013652) | | pancreatic insulinoma, non-human animal (MONDO:1013585) | | spinal meningioma, non-human animal (MONDO:1013097) | | Stargardt disease, fat sand rat (MONDO:7770555) | | kidney fibrosarcoma, non-human animal (MONDO:1013342) | | agenesis of corpus callosum, goat (MONDO:7770628) | | sterile, cattle (MONDO:7770399) | | retroperitoneal neoplasm, non-human animal (MONDO:1013147) | | lymphadenitis, non-human animal (MONDO:1013590) | | disseminated intravascular coagulation, non-human animal (MONDO:1013048) | | translocation chromosomal structural anomaly, water buffalo (MONDO:7770659) | | anencephaly/exencephaly, dog (MONDO:7770402) | | male subfertility, zebu cattle (MONDO:7770563) | | plasmacytoma, non-human animal (MONDO:1013722) | | acute epiglottitis, non-human animal (MONDO:1013415) | | anaphylaxis, non-human animal (MONDO:1013548) | | hyperbilirubinaemia, SLCO1B3-related, sheep (MONDO:7770299) | | anthrax infection, non-human animal (MONDO:1013673) | | acute myeloid leukemia, non-human animal (MONDO:1013327) | | tooth disorder, non-human animal (MONDO:1013389) | | cleft lip, dog (MONDO:7770224) | | sex chromosome difference of sexual development, water buffalo (MONDO:7770343) | | in situ carcinoma, non-human animal (MONDO:1013274) | | disease of primarily extrinsic mechanism, non-human animal (MONDO:7770016) | | nasal cavity carcinoma in situ, non-human animal (MONDO:1013283) | | arthritic joint disease, non-human animal (MONDO:1013736) | | brachycephaly, cattle (MONDO:7770387) | | anus neoplasm, non-human animal (MONDO:1013112) | | disease by etiologic mechanism, non-human animal (MONDO:7770014) | | eosinophilic gastroenteritis, non-human animal (MONDO:1013416) | | inflammatory bowel disease, dog (MONDO:7770067) | | eye defects, domestic cat (MONDO:7770651) | | monorchidism, dog (MONDO:7770741) | | glycogen storage disease II, zebu cattle (MONDO:7770359) | | prognathism, sheep (MONDO:7770727) | | basal cell carcinoma, non-human animal (MONDO:1013333) | | primary prostate urothelial carcinoma, non-human animal (MONDO:1013368) | | essential thrombocythemia, non-human animal (MONDO:1013361) | | Lyme disease, non-human animal (MONDO:1013091) | | adrenoleukodystrophy, rabbit (MONDO:7770612) | | lower limb hyperextension, goat (MONDO:7770736) | | gallbladder adenoma, non-human animal (MONDO:1013314) | | split cord malformation type II (MONDO:1060221) | | lymphocytic gastritis, non-human animal (MONDO:1013062) | | hypersplenism, non-human animal (MONDO:1013689) | | Thomsen and Becker disease, non-human animal (MONDO:1013109) | | neoplasm of testis, non-human animal (MONDO:1013155) | | cleft lip and jaw, bilateral, cattle (MONDO:7770246) | | obesity, domestic cat (MONDO:7770113) | | sex chromosome difference of sexual development, dog (MONDO:7770348) | | inflammatory bowel disease, guinea pig (MONDO:7770464) | | myelodysplastic syndrome, non-human animal (MONDO:1013105) | | cornea neoplasm, non-human animal (MONDO:1013428) | | pulmonary fibrosis, non-human animal (MONDO:1013197) | | erysipelas, non-human animal (MONDO:1013678) | | congenital stationary night blindness, GRM6-related, horse (MONDO:7770231) | | chronic gastritis, non-human animal (MONDO:1013060) | | atrioventricular septal defect, non-human animal (MONDO:1013065) | | translocation chromosomal structural anomaly, sheep (MONDO:7770664) | | Parkinson disease, dog (MONDO:7770166) | | progressive retinal, central, and peripheral neurodegeneration, PCYT2-related, dog (MONDO:7770268) | | lumbar spinal stenosis, non-human animal (MONDO:1013212) | | cranial nerve neuropathy, non-human animal (MONDO:1013038) | | trichofolliculoma, non-human animal (MONDO:1013639) | | omphallorhagia, cattle (MONDO:7770390) | | central nervous system neoplasm, non-human animal (MONDO:1013251) | | hypomyelinating polyneuropathy, MTMR2-related, dog (MONDO:7770266) | | brachygnathia superior, white-tailed deer (MONDO:7770489) | | heart neoplasm, non-human animal (MONDO:1013118) | | delayed postoperative hemorrhage, dog (MONDO:7770174) | | hypopituitarism, non-human animal (MONDO:1013583) | | adrenal gland cancer, non-human animal (MONDO:1013111) | | thiamine deficiency non-human animal (MONDO:1013220) | | spondyloocular syndrome, medaka (MONDO:7770237) | | pleuropneumonia, non-human animal (MONDO:1013662) | | pancreatitis, non-human animal (MONDO:1013602) | | orbit neoplasm, non-human animal (MONDO:1013134) | | constipation disorder, non-human animal (MONDO:1013567) | | compartment syndrome, non-human animal (MONDO:1013032) | | chromosomal abnormality, houbara bustard (MONDO:7770541) | | cheilitis, non-human animal (MONDO:1013560) | | polioencephalopathy, MECR-related, dog (MONDO:7770412) | | hypertrophic pyloric stenosis, non-human animal (MONDO:1013253) | | vena cava defect, domestic cat (MONDO:7770370) | | polyp of middle ear, non-human animal (MONDO:1013191) | | pica disease, non-human animal (MONDO:1013667) | | escherichia coli infection, non-human animal (MONDO:1013059) | | uveitis, non-human animal (MONDO:1013754) | | liver abscess (disease), non-human animal (MONDO:1013000) | | duplication chromosomal structural anomaly, cattle (MONDO:7770657) | | ulcerative stomatitis, non-human animal (MONDO:1013216) | | acute respiratory distress syndrome, non-human animal (MONDO:1013004) | | viral encephalitis, non-human animal (MONDO:1013508) | | thyrotoxicosis, non-human animal (MONDO:1013621) | | squamous papilloma, non-human animal (MONDO:1013460) | | neurofibrosarcoma, non-human animal (MONDO:1013634) | | urinary bladder carcinoma, non-human animal (MONDO:1013299) | | meconium aspiration syndrome, non-human animal (MONDO:1013424) | | necrotizing hypophysitis (MONDO:1060219) | | ataxia, middle-African hedgehog (MONDO:7770241) | | cellulitis, non-human animal (MONDO:1013558) | | brachygnathia, giraffe (MONDO:7770251) | | corneal ulceration, dog (MONDO:7770188) | | food allergy, non-human animal (MONDO:1013076) | | liposarcoma, non-human animal (MONDO:1013588) | | exostosis, non-human animal (MONDO:1013761) | | ectodermal dysplasia, pig (MONDO:7770104) | | plasminogen activator inhibitor-1 deficiency, SERPINE1-related, dog (MONDO:7770629) | | atrial flutter, non-human animal (MONDO:1013244) | | polyp, non-human animal (MONDO:1013723) | | chromosomal abnormality, chicken (MONDO:7770537) | | myelitis, non-human animal (MONDO:1013596) | | discoid lupus erythematosus, non-human animal (MONDO:1013047) | | carcinoma of esophagus, non-human animal (MONDO:1013286) | | parvalbumin fish allergen, rainbow trout (MONDO:7770599) | | varicocele, non-human animal (MONDO:1013666) | | haplotype with homozygous deficiency, NOA1-related, cattle (MONDO:7770515) | | primary ciliary dyskinesia, STK36-related, dog (MONDO:7770170) | | stomatocytosis, dog (MONDO:7770582) | | progeroid syndrome, naked mole-rat (MONDO:7770715) | | renal pelvis urothelial carcinoma, non-human animal (MONDO:1013369) | | exophthalmos, non-human animal (MONDO:1013674) | | motion sickness, non-human animal (MONDO:1013378) | | parasitic myositis, non-human animal (MONDO:1013426) | | sex chromosome difference of sexual development, wood lemming (MONDO:7770336) | | central nervous system disorder, non-human animal (MONDO:1013242) | | chromosomal structural anomaly, translocation, centric fusion, American beaver (MONDO:7770671) | | benign essential blepharospasm, non-human animal (MONDO:1013669) | | benign neoplasm, non-human animal (MONDO:1013110) | | nephronophthisis, dog (MONDO:7770581) | | avian influenza, non-human animal (MONDO:1013491) | | hyalitis, non-human animal (MONDO:1013701) | | vena cava defect, dog (MONDO:7770371) | | muscle weakness, CACNA1S-related, cattle (MONDO:7770417) | | mucopolysaccharidosis, non-human animal (MONDO:1013675) | | cardiac defects, medaka (MONDO:7770295) | | basosquamous carcinoma, non-human animal (MONDO:1013334) | | progressive retinal atrophy, GTPBP2-related, dog (MONDO:7770578) | | spinal muscular atrophy, pig (MONDO:7770357) | | urinary bladder neoplasm, non-human animal (MONDO:1013161) | | chromosomal abnormality, domestic cat (MONDO:7770272) | | sialolithiasis, non-human animal (MONDO:1013616) | | endocarditis, non-human animal (MONDO:1013741) | | phlebitis, non-human animal (MONDO:1013661) | | brachygnathia, white-tailed deer (MONDO:7770488) | | primary central nervous system lymphoma, non-human animal (MONDO:1013092) | | small intestine leiomyoma, non-human animal (MONDO:1013349) | | bladder squamous cell carcinoma, non-human animal (MONDO:1013459) | | anal polyp, non-human animal (MONDO:1013190) | | adactyly, rhesus macaque (MONDO:7770211) | | vertebral anomalies, horse (MONDO:7770531) | | chromosomal structural anomaly, translocation, centric fusion, common shrew (MONDO:7770679) | | mummified fetus, pig (MONDO:7770300) | | cystic ovary, domestic cat (MONDO:7770702) | | neuronal ceroid lipofuscinosis, rhesus macaque (MONDO:7770502) | | peritoneal neoplasm, non-human animal (MONDO:1013259) | | dientamoebiasis, non-human animal (MONDO:1013538) | | methemoglobinemia, dog (MONDO:7770487) | | congenital heart defect, zebu cattle (MONDO:7770640) | | infertility disorder, non-human animal (MONDO:1013653) | | diverticulitis, non-human animal (MONDO:1013694) | | ependymal tumor of brain, non-human animal (MONDO:1013054) | | cavernous hemangioma, non-human animal (MONDO:1013475) | | uterine aplasia, horse (MONDO:7770427) | | leiomyoma, non-human animal (MONDO:1013715) | | ophthalmoplegia, non-human animal (MONDO:1013601) | | skin carcinoma in situ, non-human animal (MONDO:1013273) | | equine odontoclastic tooth resorption and hypercementosis, horse (MONDO:7770365) | | uterine aplasia, dog (MONDO:7770425) | | difference of sexual development, chicken (MONDO:7770331) | | amelia, dog (MONDO:7770407) | | chromosomal structural anomaly, translocation, centric fusion, pink salmon (MONDO:7770678) | | cystic ovary, medaka (MONDO:7770292) | | deficiency color vision, medaka (MONDO:7770317) | | craniofacial deformities, Nile tilapia (MONDO:7770233) | | adamantinoma, non-human animal (MONDO:1013767) | | osteoarthritis, hip, non-human animal (MONDO:1013170) | | bacterial endocarditis, non-human animal (MONDO:1013052) | | conjunctivitis, non-human animal (MONDO:1013738) | | obesity, horse (MONDO:7770114) | | paranasal sinus carcinoma, non-human animal (MONDO:1013474) | | cystinuria, maned wolf (MONDO:7770419) | | tricuspid valve stenosis, non-human animal (MONDO:1013229) | | kidney carcinoma in situ, non-human animal (MONDO:1013290) | | bone fracture, non-human animal (MONDO:1013743) | | cervicitis, non-human animal (MONDO:1013645) | | rectum lymphoma, non-human animal (MONDO:1013365) | | tetraploidy polyploidy, chicken (MONDO:7770682) | | chronic rhinosinusitis, non-human animal (MONDO:1013450) | | polyneuritis, non-human animal (MONDO:1013608) | | sweat gland neoplasm, non-human animal (MONDO:1013153) | | laryngitis, non-human animal (MONDO:1013586) | | portal hypertension, non-human animal (MONDO:1013545) | | wry nose, giraffe (MONDO:7770252) | | dental abnormalities, fox (MONDO:7770376) | | leiomyosarcoma, non-human animal (MONDO:1013716) | | tonsil neoplasm, non-human animal (MONDO:1013158) | | heart lymphoma, non-human animal (MONDO:1013363) | | gonadal dysgenesis, non-human animal (MONDO:1013417) | | chronic ulcer of skin, non-human animal (MONDO:1013077) | | frostbite, non-human animal (MONDO:1013650) | | blepharitis, non-human animal (MONDO:1013552) | | dyskinesia of esophagus, non-human animal (MONDO:1013166) | | gastric neoplasm, non-human animal (MONDO:1013122) | | auditory-pigmentary syndrome, PAX3-related, horse (MONDO:7770070) | | liver fibrosarcoma, non-human animal (MONDO:1013341) | | anterior segment dysgenesis, dog (MONDO:7770181) | | cataract, green monkey (MONDO:7770274) | | tendon sheath disorder, non-human animal (MONDO:1013461) | | Sjogren syndrome, dog (MONDO:7770551) | | mammary gland abnormality, sheep (MONDO:7770196) | | botulism, non-human animal (MONDO:1013554) | | hypertensive encephalopathy, non-human animal (MONDO:1013051) | | cerebellar abiotrophy, CACNA2D2-related, cattle (MONDO:7770706) | | focal epilepsy, non-human animal (MONDO:1013055) | | colon carcinoma, non-human animal (MONDO:1013276) | | multiple organ dysfunction syndrome, non-human animal (MONDO:1013102) | | pontocerebellar hypoplasia, AMPD2-related, dog (MONDO:7770454) | | albinism skin color, goldfish (MONDO:7770169) | | fetal death, pig (MONDO:7770377) | | transmission ratio distortion, zebu cattle (MONDO:7770296) | | myelophthisic anemia, non-human animal (MONDO:1013469) | | carbuncle, non-human animal (MONDO:1013644) | | embryonic lethality, cattle (MONDO:7770446) | | persistent hyperplastic primary vitreous, non-human animal (MONDO:1013526) | | viral pneumonia, non-human animal (MONDO:1013438) | | lip disorder, non-human animal (MONDO:1013422) | | enophthalmos, non-human animal (MONDO:1013696) | | fatty metamorphosis of viscera, rabbit (MONDO:7770579) | | stromal corneal dystrophy, non-human animal (MONDO:1013036) | | congenital esophageal achalasia, horse (MONDO:7770738) | | circadian disruption, macaque (MONDO:7770194) | | pulmonary valve dysplasia, dog (MONDO:7770270) | | xanthomatous hypophysitis (MONDO:1060217) | | inherited torticollis, non-human animal (MONDO:1013711) | | cysticercosis, non-human animal (MONDO:1013676) | | cardiogenic shock, non-human animal (MONDO:1013533) | | sex chromosome difference of sexual development, domestic cat (MONDO:7770329) | | testicular disorder, non-human animal (MONDO:1013257) | | small intestine adenocarcinoma, non-human animal (MONDO:1013272) | | MIR137-related neurodevelopmental disorder, pig (MONDO:7770496) | | elliptocytosis, dog (MONDO:7770221) | | Sjogren syndrome, domestic cat (MONDO:7770552) | | diphtheria, non-human animal (MONDO:1013494) | | intermittent vascular claudication, non-human animal (MONDO:1013243) | | acute kidney injury, non-human animal (MONDO:1013530) | | cerebral infarction, non-human animal (MONDO:1013024) | | diabetes mellitus, HNF1A-related, pig (MONDO:7770517) | | hypervitaminosis D, non-human animal (MONDO:1013500) | | ectopic paw pads, domestic cat (MONDO:7770195) | | urachal diverticulum, non-human animal (MONDO:1013536) | | claw/hoof disorders, zebu cattle (MONDO:7770312) | | nasolacrimal duct obstruction, dog (MONDO:7770475) | | sex chromosome difference of sexual development, goat (MONDO:7770346) | | caudal articular process dysplasia, dog (MONDO:7770193) | | aortic aneurysm, non-human animal (MONDO:1013013) | | skin carcinoma, non-human animal (MONDO:1013292) | | deficiency color vision, macaque (MONDO:7770226) | | hypothalamic hamartoma, dog (MONDO:7770632) | | erythema multiforme, non-human animal (MONDO:1013058) | | shoulder luxation, alpaca (MONDO:7770431) | | Meier-Gorlin syndrome 10 (MONDO:0981050) | | synchronic limb movement, EFNB3-related, dog (MONDO:7770625) | | ovarian lymphoma, non-human animal (MONDO:1013423) | | sebaceous gland dysplasia, SOAT1-related, domestic cat (MONDO:7770212) | | sex chromosome difference of sexual development, bighorn sheep (MONDO:7770689) | | nephronophthisis, domestic cat (MONDO:7770580) | | cystic microphthalmia, dog (MONDO:7770559) | | aniridia, non-human animal (MONDO:1013672) | | sex chromosome difference of sexual development, gray short-tailed opossum (MONDO:7770341) | | phototoxic dermatitis, non-human animal (MONDO:1013571) | | hypohidrotic ectodermal dysplasia, X-linked, EDA-related, domestic cat (MONDO:7770500) | | bursitis, non-human animal (MONDO:1013734) | | monkeypox, non-human animal (MONDO:1013503) | | pyelonephritis, non-human animal (MONDO:1013613) | | spondylolisthesis, non-human animal (MONDO:1013766) | | sex chromosome monosomy, donkey (MONDO:7770710) | | caudal and thoracic vertebral and viscerocranial malformation, SLC40A1-related, cattle (MONDO:7770699) | | peripheral nervous system neoplasm, non-human animal (MONDO:1013139) | | gray coat color, STX17-related, horse (MONDO:7770052) | | neoplasm of esophagus, non-human animal (MONDO:1013132) | | hemosiderosis, non-human animal (MONDO:1013688) | | arrhythmogenic left ventricular cardiomyopathy, dog (MONDO:7770163) | | peracute mortality syndrome, red panda (MONDO:7770554) | | spinal cord injury, non-human animal (MONDO:1013211) | | central congenital hypothyroidism, non-human animal (MONDO:1013512) | | scrapie, non-human animal (MONDO:1013681) | | uterine aplasia, rabbit (MONDO:7770423) | | ataxia with isolated vitamin E deficiency, TTPA-related, dog (MONDO:7770574) | | mitral valve prolapse, non-human animal (MONDO:1013100) | | glanders, non-human animal (MONDO:1013651) | | salpingitis, non-human animal (MONDO:1013663) | | leg weakness, mallard (MONDO:7770434) | | Parkinson disease, rhesus macaque (MONDO:7770285) | | eosinophilic gastritis, non-human animal (MONDO:1013539) | | traumatic brain injury, non-human animal (MONDO:1013018) | | chromosomal structural anomaly, translocation, centric fusion, sheep (MONDO:7770666) | | sex chromosome difference of sexual development, sheep (MONDO:7770339) | | vaginal neoplasm, non-human animal (MONDO:1013162) | | scrotum neoplasm, non-human animal (MONDO:1013148) | | chronic endometritis, non-human animal (MONDO:1013510) | | lens subluxation, non-human animal (MONDO:1013087) | | cryptosporidiosis, non-human animal (MONDO:1013569) | | brain stem infarction, non-human animal (MONDO:1013019) | | ectodermal dysplasia, edaradd-related, mangrove rivulus (MONDO:7770725) | | double outlet right ventricle, non-human animal (MONDO:1013067) | | euthyroid sick syndrome, non-human animal (MONDO:1013534) | | nerve sheath neoplasm, non-human animal (MONDO:1013140) | | lymphocyte intestinal retention defect, ITGB7-related, cattle (MONDO:7770513) | | chromosomal abnormality, dog (MONDO:7770273) | | tracheal cancer, non-human animal (MONDO:1013159) | | coloboma of eyelid, non-human animal (MONDO:1013479) | | dominant white coat color, KIT-related, horse (MONDO:7770054) | | heart failure, non-human animal (MONDO:1013068) | | infertility, macaque (MONDO:7770650) | | histoplasmosis, non-human animal (MONDO:1013700) | | polydactyly, ALX4-related, dog (MONDO:1013785) | | enteritis, non-human animal (MONDO:1013576) | | corneal disorder, non-human animal (MONDO:1013388) | | muscle hypertrophy, dysphagia, and gait abnormalities, dog (MONDO:7770455) | | XY sex reversal, medaka (MONDO:7770333) | | vaginal leiomyoma, non-human animal (MONDO:1013352) | | lissencephaly, cattle (MONDO:7770321) | | osteomyelitis, non-human animal (MONDO:1013747) | | skeletal dysplasia, FGD3-related, cattle (MONDO:7770172) | | megaoesophagus, MCHR2-related, dog (MONDO:7770255) | | polydactyly, SHH-related, dog (MONDO:1013784) | | leukodystrophy, CYTB-related, dog (MONDO:7770223) | | chromosomal structural anomaly, translocation, centric fusion, European plaice (MONDO:7770677) | | meningeal neoplasm, non-human animal (MONDO:1010206) | | cholestasis, non-human animal (MONDO:1013564) | | left ventricular noncompaction cardiomyopathy, guinea pig (MONDO:7770586) | | hydronephrosis, non-human animal (MONDO:1013580) | | lymph node neoplasm, non-human animal (MONDO:1013127) | | acute erythroid leukemia, non-human animal (MONDO:1013358) | | brain disorder, non-human animal (MONDO:1013017) | | gastroesophageal reflux disease, non-human animal (MONDO:1013063) | | sex chromosome trisomy, XXY, Agile wallaby (MONDO:7770647) | | abscess, non-human animal (MONDO:1013735) | | radial neuropathy, non-human animal (MONDO:1013182) | | dilated cardiomyopathy, LMNA-related, macaque (MONDO:7770445) | | adenoma of pancreas, non-human animal (MONDO:1013316) | | periodic fever syndrome, HAS2-related, dog (MONDO:1013791) | | esophagus carcinoma in situ, non-human animal (MONDO:1013287) | | testicular agenesis, dog (MONDO:7770168) | | nephrogenic diabetes insipidus, non-human animal (MONDO:1013046) | | thyroid crisis, non-human animal (MONDO:1013223) | | feline odontoclastic resorptive lesion, domestic cat (MONDO:7770366) | | multiple ocular defects, COL11A1-related, dog (MONDO:7770411) | | paradoxical pseudomyotonia, SLC7A10-related, dog (MONDO:7770191) | | synovitis, non-human animal (MONDO:1013619) | | trachea leiomyoma, non-human animal (MONDO:1013350) | | posthitis, non-human animal (MONDO:1013680) | | neoplasm of jaw, non-human animal (MONDO:1013267) | | rectum adenoma, non-human animal (MONDO:1013319) | | hypercholesterolaemia, macaque (MONDO:7770323) | | acute otitis externa, non-human animal (MONDO:1013172) | | gastric leiomyosarcoma, non-human animal (MONDO:1013355) | | anal margin squamous cell carcinoma, non-human animal (MONDO:1013215) | | chromosomal structural anomaly, translocation, centric fusion, Atlantic cod (MONDO:7770676) | | XY sex reversal, sheep (MONDO:7770335) | | ascites, cockatiel (MONDO:7770031) | | secondary neoplasm, non-human animal (MONDO:1013523) | | phacoanaphylactic uveitis, non-human animal (MONDO:1013236) | | ptosis, non-human animal (MONDO:1013612) | | bone fibrosarcoma, non-human animal (MONDO:1013340) | | nasolacrimal duct obstruction, horse (MONDO:7770476) | | paroxysmal atrial fibrillation, non-human animal (MONDO:1013472) | | skin disorder, non-human animal (MONDO:1013399) | | Parkinson disease, pig (MONDO:7770286) | | polysaccharide storage myopathy, mule (MONDO:7770490) | | ovulatory failure, Atlantic salmon (MONDO:7770607) | | first-degree atrioventricular block, non-human animal (MONDO:1013245) | | congenital cystic eye, horse (MONDO:7770560) | | thecoma, non-human animal (MONDO:1013638) | | toxic polyneuropathy, non-human animal (MONDO:1013189) | | RNU12-related minor spliceopathy disorder (MONDO:1060223) | | listeriosis, non-human animal (MONDO:1013589) | | chromosomal structural anomaly, translocation, centric fusion, dog (MONDO:7770668) | | cornea squamous cell carcinoma, non-human animal (MONDO:1013455) | | male subfertility, Nile tilapia (MONDO:7770522) | | dermoid cyst, non-human animal (MONDO:1013390) | | sporotrichosis, non-human animal (MONDO:1013665) | | leiomyosarcoma of the corpus uteri, non-human animal (MONDO:1013356) | | seminoma, non-human animal (MONDO:1013615) | | panniculitis, non-human animal (MONDO:1013604) | | oligospermia, non-human animal (MONDO:1013709) | | scurvy, non-human animal (MONDO:1013501) | | thyroid cancer, non-human animal (MONDO:1013156) | | brachygnathia superior, domestic cat (MONDO:7770405) | | XX difference of sexual development, cattle (MONDO:7770532) | | neurodevelopmental disorder with seizures and impaired intellectual and language development (MONDO:0981032) | | ovarian cyst, non-human animal (MONDO:1013174) | | sex chromosome difference of sexual development, Przewalski's horse (MONDO:7770494) | | isolated optic nerve hypoplasia, non-human animal (MONDO:1013524) | | peliosis hepatis, non-human animal (MONDO:1013260) | | haplotype with homozygous deficiency HH1, zebu cattle (MONDO:7770383) | | synovium neoplasm, non-human animal (MONDO:1013154) | | brachial plexus neuropathy, non-human animal (MONDO:1013386) | | anencephaly/exencephaly, brown bear (MONDO:7770403) | | immature cataract, non-human animal (MONDO:1013023) | | oculocutaneous albinism, Japanese raccoon dog (MONDO:7770118) | | amorphus globosus, goat (MONDO:7770391) | | vagina leiomyosarcoma, non-human animal (MONDO:1013357) | | pulmonary emphysema, non-human animal (MONDO:1013196) | | retinitis pigmentosa 101 (MONDO:0981164) | | microcephaly, ferret (MONDO:7770524) | | chromosomal abnormality, horse (MONDO:7770420) | | disease by body system or component, non-human animal (MONDO:7770012) | | hypercholesterolaemia, LDLR-related and MBTPS2-related, rhesus macaque (MONDO:7770236) | | salivary gland disorder, non-human animal (MONDO:1013381) | | junctional epidermolysis bullosa, ITGA6-related, cattle (MONDO:7770259) | | anterior uveitis, non-human animal (MONDO:1013235) | | Leigh syndrome, NDUFS7-related, dog (MONDO:7770456) | | autosomal dominant nonsyndromic hearing loss 91 (MONDO:0981166) | | eye lymphoma, non-human animal (MONDO:1013094) | | cor pulmonale, non-human animal (MONDO:1013033) | | chromosomal structural anomaly, translocation, centric fusion, pig (MONDO:7770667) | | congestive heart failure, non-human animal (MONDO:1013391) | | dental abnormalities, dog (MONDO:7770432) | | dentigerous cyst, non-human animal (MONDO:1013412) | | dyplasias with multiple joint dislocations, cattle (MONDO:7770705) | | cerebellar abiotrophy, MUTYH-related, horse (MONDO:1013780) | | granulosa cell tumor, non-human animal (MONDO:1013343) | | posterior uveitis, non-human animal (MONDO:1013237) | | macrothrombocytopenia, dog (MONDO:7770098) | | ovarian adenocarcinoma, non-human animal (MONDO:1013405) | | tongue neoplasm, non-human animal (MONDO:1013157) | | hamartoma, non-human animal (MONDO:1013631) | | hypertrophic cardiomyopathy, MYH6-related, pig (MONDO:7770610) | | encephalomyelitis, non-human animal (MONDO:1013647) | | ovarian cystadenoma, non-human animal (MONDO:1013338) | | chromosomal abnormality, Japanese quail (MONDO:7770539) | | ankylosis, non-human animal (MONDO:1013549) | | heterotopic ossification, gray parrot (MONDO:7770199) | | lung disorder, non-human animal (MONDO:1013090) | | epiglottitis, non-human animal (MONDO:1013648) | | hernia, koala (MONDO:7770619) | | hemoglobinuria, non-human animal (MONDO:1013699) | | cataract and non-ketotic hyperglycinemia, grivet (MONDO:7770091) | | kidney neoplasm, non-human animal (MONDO:1013146) | | hypomyelinating polyneuropathy, SH3TC2-related, dog (MONDO:7770277) | | white spotting coat colour, MITF-related, horse (MONDO:7770069) | | actinomycosis, non-human animal (MONDO:1013487) | | achondroplasia, PRICKLE1-related, sheep (MONDO:7770232) | | ventricular fibrillation, non-human animal (MONDO:1013537) | | myxoma, non-human animal (MONDO:1013720) | | pilomatrixoma, non-human animal (MONDO:1013636) | | heart valve disorder, non-human animal (MONDO:1013069) | | severe combined immunodeficiency disease, IL2RG and, RAG1-related, crab-eating macaque (MONDO:7770313) | | urethra squamous cell carcinoma, non-human animal (MONDO:1013458) | | oculocutaneous albinism, cane toad (MONDO:7770653) | | choroid plexus papilloma, non-human animal (MONDO:1013477) | | double-outlet right ventricle, goat (MONDO:7770229) | | xanthomatosis, non-human animal (MONDO:1013691) | | polyploidy, sheep (MONDO:7770687) | | aortic valve stenosis, dog (MONDO:7770584) | | anencephaly/exencephaly, domestic cat (MONDO:7770401) | | chronic cystitis, non-human animal (MONDO:1013040) | | Parkinson disease, turquoise killifish (MONDO:7770395) | | hair follicle neoplasm, non-human animal (MONDO:1013123) | | proctitis, non-human animal (MONDO:1013610) | | male subfertility, AK9-related, cattle (MONDO:7770364) | | XX difference of sexual development, Japanese flounder (MONDO:7770281) | | megalocornea, non-human animal (MONDO:1013705) | | episodic ataxia, dog (MONDO:7770550) | | brain neoplasm, non-human animal (MONDO:1013117) | | spongiform myelopathy, cattle (MONDO:7770028) | | bladder leiomyoma, non-human animal (MONDO:1013351) | | epididymitis, non-human animal (MONDO:1013697) | | nasolacrimal duct obstruction, domestic cat (MONDO:7770478) | | panophthalmitis, non-human animal (MONDO:1013710) | | hyperinsulinism, non-human animal (MONDO:1013582) | | chronic eosinophilic leukemia, non-human animal (MONDO:1013360) | | bordetellosis, non-human animal (MONDO:1013553) | | tail abnormalities, cattle (MONDO:7770483) | | respiratory failure, non-human animal (MONDO:1013204) | | deficiency color vision, common marmoset (MONDO:7770225) | | dermoid cyst of skin, non-human animal (MONDO:1013044) | | laryngeal granuloma, non-human animal (MONDO:1013515) | | schwannoma, non-human animal (MONDO:1013635) | | claw/hoof disorders, horse (MONDO:7770398) | | adrenal cortex adenoma, non-human animal (MONDO:1013313) | | ataxia, lion (MONDO:7770527) | | hypersensitivity pneumonitis, non-human animal (MONDO:1013768) | | asthenoteratozoospermia, macaque (MONDO:7770175) | | bacterial arthritis, non-human animal (MONDO:1013383) | | disease of genetic or genomic mechanism, non-human animal (MONDO:7770015) | | epidermolytic hyperkeratosis, walrus (MONDO:7770316) | | eye defects, black-footed ferret (MONDO:7770314) | | lymphangioma, non-human animal (MONDO:1013591) | | microcephaly, YIPF5-related, rabbit (MONDO:7770227) | | chromosomal abnormality, chukar partridge (MONDO:7770540) | | hip dysplasia, horse (MONDO:7770535) | | Bacteroides infectious disease, non-human animal (MONDO:1013492) | | cataract, donkey (MONDO:7770200) | | cardiac arrest, non-human animal (MONDO:1013022) | | liver cancer, non-human animal (MONDO:1013124) | | esophageal squamous cell carcinoma, non-human animal (MONDO:1013457) | | gastric lymphoma, non-human animal (MONDO:1013093) | | alopecia, American red squirrel (MONDO:7770260) | | morbid obesity, non-human animal (MONDO:1013165) | | Proteus infectious disease, non-human animal (MONDO:1013504) | | cataract, American black bear (MONDO:7770743) | | haplotype with homozygous deficiency, SLC33A1-related, sheep (MONDO:7770501) | | diaphragmatic hernia, alpaca (MONDO:7770397) | | lipid storage disease, superb bird-of-paradise (MONDO:7770362) | | myositis disease, non-human animal (MONDO:1013746) | | clumped feathers, high-stress reactivity, and tameness, Australian zebra finch (MONDO:7770451) | | nasal dermal arteritis, dog (MONDO:7770245) | | placental insufficiency, non-human animal (MONDO:1013527) | | albinism, non-human animal (MONDO:1013670) | | neoplasm of mediastinum, non-human animal (MONDO:1013128) | | bacterial urinary tract infection, non-human animal (MONDO:1013234) | | neoplasm of neck, non-human animal (MONDO:1013131) | | ossifying fibroma, non-human animal (MONDO:1013395) | | Usher syndrome, rabbit (MONDO:7770171) | | long QT syndrome, KCNQ1-related, dog (MONDO:7770288) | | XX difference of sexual development, guppy (MONDO:7770379) | | translocation chromosomal structural anomaly, pig (MONDO:7770662) | | urinary tract infection, non-human animal (MONDO:1013233) | | cor triatriatum sinister, non-human animal (MONDO:1013066) | | eosinophilic pneumonia, non-human animal (MONDO:1013529) | | dental abnormalities, sheep (MONDO:7770621) | | T cell deficiency, chicken (MONDO:7770325) | | thoracolumbar myelopathy, dog (MONDO:7770185) | | colon carcinoma in situ, non-human animal (MONDO:1013277) | | median nerve neuropathy, non-human animal (MONDO:1013435) | | lissencephaly, domestic cat (MONDO:7770320) | | atresia ani, dog (MONDO:7770453) | | lymphedema, non-human animal (MONDO:1013592) | | ethylene glycol poisoning, non-human animal (MONDO:1013081) | | nocardiosis, non-human animal (MONDO:1013657) | | progressive retinal atrophy, GUCY2D-related, dog (MONDO:7770192) | | lameness, chicken (MONDO:7770257) | | polyploidy, rabbit (MONDO:7770686) | | primordial disproportionate dwarfism, PRDM10-related, cattle (MONDO:7770696) | | chondrodysplasia, American black bear (MONDO:7770498) | | silver coat color, PMEL-related, horse (MONDO:7770059) | | Parkinson disease, white-tufted-ear marmoset (MONDO:7770248) | | Zollinger-Ellison syndrome, non-human animal (MONDO:1013241) | | cataract, grivet (MONDO:7770097) | | haplotype with homozygous deficiency JBH17, CDC45-related, cattle (MONDO:7770173) | | Fanconi syndrome, FAN1-related, dog (MONDO:7770222) | | labyrinthitis, non-human animal (MONDO:1013463) | | thoracoabdominal syndrome, dog (MONDO:7770269) | | ileus, non-human animal (MONDO:1013769) | | cor triatriatum sinister, domestic cat (MONDO:7770615) | | tracheal stenosis, non-human animal (MONDO:1013226) | | granulomatous gastritis, non-human animal (MONDO:1013540) | | staphylococcus aureus infection, non-human animal (MONDO:1013535) | | cerebrovascular disorder, non-human animal (MONDO:1013026) | | polydactyly, LMBR1-related, domestic cat (MONDO:1013787) | | microphthalmia with hematopoietic defects, DNAJC21-related, dog (MONDO:7770467) | | PDCD1-related immune system disorder, pig (MONDO:7770472) | | pericardial effusion, non-human animal (MONDO:1013397) | | chronic pancreatitis, non-human animal (MONDO:1013178) | | oculocutaneous albinism, OCA2-related, rhesus macaque (MONDO:7770290) | | parathyroid gland adenoma, non-human animal (MONDO:1013317) | | injury, non-human animal (MONDO:1013377) | | disease by developmental or physiological process, non-human animal (MONDO:7770013) | | adactyly, pig (MONDO:7770305) | | cystitis, non-human animal (MONDO:1013570) | | endometriosis, non-human animal (MONDO:1013695) | | rectum leiomyoma, non-human animal (MONDO:1013348) | | gallbladder neoplasm, non-human animal (MONDO:1013121) | | inflammatory bowel disease, non-human animal (MONDO:1013080) | | urethral obstruction, non-human animal (MONDO:1013231) | | acute pancreatitis, non-human animal (MONDO:1013177) | | gamatogenic failure, medaka (MONDO:7770605) | | giardiasis, non-human animal (MONDO:1013578) | | polyendocrine syndrome, dog (MONDO:7770380) | | frontotemporal dementia, macaque (MONDO:7770324) | | interstitial nephritis, non-human animal (MONDO:1013262) | | multilocular clear cell renal cell carcinoma, non-human animal (MONDO:1013337) | | renal carcinoma, non-human animal (MONDO:1013289) | | cervicothoracic vertebral malformation, horse (MONDO:7770381) | | muscular hypertrophy (double muscling), yellow catfish (MONDO:7770374) | | lymph node aplasia, sheep (MONDO:7770262) | | mediastinitis, non-human animal (MONDO:1013593) | | pasteurellosis, non-human animal (MONDO:1013659) | | orbital cellulitis, non-human animal (MONDO:1013169) | | cor triatriatum sinister, goat (MONDO:7770228) | | refeeding syndrome, non-human animal (MONDO:1013203) | | xanthogranulomatous hypophysitis (MONDO:1060218) | | congenital partial colonic agenesis, horse (MONDO:7770353) | | translocation chromosomal structural anomaly, pink salmon (MONDO:7770663) | | colorectal adenoma, non-human animal (MONDO:1013315) | | cholelithiasis, non-human animal (MONDO:1013563) | | esophagus leiomyoma, non-human animal (MONDO:1013346) | | achondrogenesis, COL2A1-related, sheep (MONDO:7770693) | | epithelial neoplasm, non-human animal (MONDO:1013729) | | cystic ovary, dog (MONDO:7770703) | | prognathism, European seabass (MONDO:7770457) | | larynx carcinoma in situ, non-human animal (MONDO:1013281) | | pleural empyema, non-human animal (MONDO:1013572) | | sarcoidosis, non-human animal (MONDO:1013664) | | non-epidermolytic ichthyosis, SDR9C7-related, dog (MONDO:7770203) | | ovarian remnant syndrome, non-human animal (MONDO:1013176) | | duplication chromosomal structural anomaly, horse (MONDO:7770658) | | candidiasis, non-human animal (MONDO:1013557) | | endocrine myopathy, non-human animal (MONDO:1013107) | | ovarian cystadenocarcinoma, non-human animal (MONDO:1013336) | | muscular dystrophy, goat (MONDO:7770575) | | urethra neoplasm, non-human animal (MONDO:1013160) | | progressive retinal atrophy, JPH2-related, dog (MONDO:7770600) | | tendinitis, non-human animal (MONDO:1013752) | | thyroid gland carcinoma, non-human animal (MONDO:1013295) | | preeclampsia, non-human animal (MONDO:1013441) | | cutaneous lupus erythematosus, non-human animal (MONDO:1013039) | | Parkinson disease, macaque (MONDO:7770626) | | dental enamel hypoplasia, non-human animal (MONDO:1013507) | | penile disorder, non-human animal (MONDO:1013396) | | meningioma, domestic cat (MONDO:7770178) | | invasive transitional cell carcinoma, BRAF-related, dog (MONDO:1013788) | | tenosynovitis, non-human animal (MONDO:1013753) | | brachygnathia, pig (MONDO:7770306) | | meningioma, wildcat (MONDO:7770177) | | thrombocytopenia, DUT-related, rabbit (MONDO:7770622) | | aplastic anemia, non-human animal (MONDO:1013010) | | sex chromosome difference of sexual development, donkey (MONDO:7770493) | | Charcot-Marie-Tooth disease, ITPR3-related, dog (MONDO:7770565) | | small intestine carcinoma, non-human animal (MONDO:1013275) | | movement disorder, non-human animal (MONDO:1013466) | | autosomal dominant hypertrophic cardiomyopathy, MYBPC3-related, domestic cat (MONDO:7770608) | | vulvar disease, non-human animal (MONDO:1013240) | | oculocutaneous albinism, medaka (MONDO:7770562) | | extraosseous osteosarcoma, non-human animal (MONDO:1013330) | | cystic ovary, guinea pig (MONDO:7770529) | | peritonitis, non-human animal (MONDO:1013679) | | leg defects, sheep (MONDO:7770327) | | mediastinal malignant lymphoma, non-human animal (MONDO:1013517) | | myelodysplastic syndrome, domestic cat (MONDO:7770512) | | psychogenic polydipsia, non-human animal (MONDO:1013195) | | pinching-off syndrome, white-tailed eagle (MONDO:7770654) | | acute liver failure, non-human animal (MONDO:1013072) | | clitoris neoplasm, non-human animal (MONDO:1013427) | | axillary neoplasm, non-human animal (MONDO:1013114) | | chromosomal structural anomaly, translocation, centric fusion, rock goby (MONDO:7770673) | | rabies, non-human animal (MONDO:1013614) | | mycotoxicosis, non-human animal (MONDO:1013654) | | nasopharyngeal neoplasm, non-human animal (MONDO:1013429) | | depigmentation syndrome, cattle (MONDO:7770649) | | infertility, golden hamster (MONDO:7770308) | | Fanconi anemia, pig (MONDO:7770734) | | babesiosis, non-human animal (MONDO:1013693) | | dilated cardiomyopathy, LMNA-related, dog (MONDO:7770375) | | GM2 gangliosidosis, HEXA-related, cattle (MONDO:7770495) | | neutrophilic dermatosis, dog (MONDO:7770611) | | split cord malformation, composite type (MONDO:1060222) | | vertebral anomalies, dog (MONDO:7770460) | | neuroaxonal dystrophy, RNF170-related, dog (MONDO:7770516) | | thrombophlebitis, non-human animal (MONDO:1013771) | | cecum adenocarcinoma, non-human animal (MONDO:1013306) | | breast adenocarcinoma, non-human animal (MONDO:1013308) | | viral respiratory tract infection, non-human animal (MONDO:1013205) | | splenic infarction, non-human animal (MONDO:1013213) | | sex chromosome trisomy, XXX, alpaca (MONDO:7770714) | | sebaceous adenocarcinoma, non-human animal (MONDO:1013270) | | REM sleep behaviour disorder, FAM8A1-related, domestic cat (MONDO:7770618) | | nephrocalcinosis, non-human animal (MONDO:1013599) | | polyglucosan storage disease, black-headed parrot (MONDO:7770543) | | sex chromosome difference of sexual development, argali (MONDO:7770690) | | cryptococcosis, non-human animal (MONDO:1013568) | | dystocia, non-human animal (MONDO:1013685) | | polycystic kidney disease, macaque (MONDO:7770742) | | chromosomal structural anomaly, translocation, centric fusion, goat (MONDO:7770665) | | meningoencephalitis, non-human animal (MONDO:1013594) | | encephalitis, non-human animal (MONDO:1013573) | | split cord malformation type I (MONDO:1060220) | | prognathism, mule (MONDO:7770499) | | enthesitis, non-human animal (MONDO:1013760) | | pericarditis, non-human animal (MONDO:1013748) | | intestinal obstruction, non-human animal (MONDO:1013392) | | chondrosarcoma, non-human animal (MONDO:1013714) | | congenital adrenal hyperplasia, common carp (MONDO:7770367) | | brachycephaly, brown trout (MONDO:7770458) | | ichthyosis, DSP-related, dog (MONDO:7770507) | | transmission ratio distortion, cattle (MONDO:7770298) | | tumor of uterus, non-human animal (MONDO:1013304) | | vaginal disorder, non-human animal (MONDO:1013238) | | conjoined twinning, chicken (MONDO:7770570) | | thoracic malformation, non-human animal (MONDO:1013453) | | squamous cell carcinoma, non-human animal (MONDO:1013268) | | tonsil carcinoma, non-human animal (MONDO:1013296) | | cataract, dog (MONDO:7770594) | | alopecia, white-tailed deer (MONDO:7770267) | | spinal muscular atrophy, KDSR-related, cattle (MONDO:7770134) | | nasal disorder, non-human animal (MONDO:1013394) | | cirrhosis of liver, non-human animal (MONDO:1013071) | | haplotype with homozygous deficiency, SEL05, SEL07, SEL18, sheep (MONDO:7770526) | | gastric adenoma, non-human animal (MONDO:1013323) | | iris neoplasm, non-human animal (MONDO:1013125) | | ovarian neoplasm, non-human animal (MONDO:1013135) | | pemphigus vulgaris, non-human animal (MONDO:1013525) | | prostatitis, non-human animal (MONDO:1013611) | | ovarian carcinoma, non-human animal (MONDO:1013303) | | skin squamous cell carcinoma, non-human animal (MONDO:1013269) | | lissencephaly, goat (MONDO:7770322) | | lethal congenital contracture syndrome 12 (MONDO:0981031) | | western equine encephalitis, non-human animal (MONDO:1013462) | | cystic kidney disease, non-human animal (MONDO:1013321) | | excessive skin folds, sheep (MONDO:7770745) | | patellar fracture and dental anomaly syndrome, domestic cat (MONDO:7770249) | | pulmonary subvalvular stenosis, non-human animal (MONDO:1013217) | | infection due to clostridium perfringens, non-human animal (MONDO:1013478) | | myxosarcoma, non-human animal (MONDO:1013721) | | contact dermatitis, non-human animal (MONDO:1013041) | | NPY2R-related nervous system disorder, medaka (MONDO:7770413) | | prostatic cyst, non-human animal (MONDO:1013194) | | eye neoplasm, non-human animal (MONDO:1013430) | | congenital portal vein hypoplasia, domestic cat (MONDO:7770722) | | pemphigus foliaceus, non-human animal (MONDO:1013180) | | chromosomal structural anomaly, translocation, centric fusion, dingo (MONDO:7770670) | | Ebstein-Bezieau neurodevelopmental syndrome (MONDO:0981163) | | primary aldosteronism, non-human animal (MONDO:1013254) | | undifferentiated pleomorphic sarcoma, non-human animal (MONDO:1013518) | | myelodysplastic syndrome, dog (MONDO:7770511) | | osteogenesis imperfecta, COL1A2-related, cattle (MONDO:7770694) | | chronic obstructive pulmonary disease, non-human animal (MONDO:1013410) | | epileptic encephalopathy, CAD-related, domestic cat (MONDO:7770591) | | ureter abnormality, dog (MONDO:7770207) | | midfacial cleft, giraffe (MONDO:7770253) | | mastitis, non-human animal (MONDO:1013745) | | coloboma of optic nerve, non-human animal (MONDO:1013481) | | conjunctival squamous cell carcinoma, non-human animal (MONDO:1013454) | | inflammatory bowel disease, pig (MONDO:7770184) | | congenital radioulnar synostosis, non-human animal (MONDO:1013218) | | hip dysplasia, roe deer (MONDO:7770302) | | epidermoid cysts, non-human animal (MONDO:1013414) | | anemia due to chronic disorder, non-human animal (MONDO:1013011) | | xanthinuria, XDH-related, domestic cat (MONDO:7770204) | | gastric carcinoma, non-human animal (MONDO:1013293) | | acquired polycythemia vera, non-human animal (MONDO:1013328) | | vulvovaginitis, non-human animal (MONDO:1013682) | | acne, non-human animal (MONDO:1013547) | | XY sex reversal, pig (MONDO:7770334) | | spermatogenic failure, QRICH2-related, cattle (MONDO:7770468) | | colorectal leiomyoma, non-human animal (MONDO:1013345) | | otitis media, non-human animal (MONDO:1013173) | | frontonasal dysplasia, ALX1-related, domestic cat (MONDO:7770256) | | ureterocele, non-human animal (MONDO:1013712) | | inflammatory bowel disease, horse (MONDO:7770220) | | asthenoteratozoospermia, northern tree shrew (MONDO:7770176) | | Arnold-Chiari malformation, domestic cat (MONDO:7770519) | | cerebral palsy, RHOB-related, rabbit (MONDO:7770505) | | chronic rhinitis, non-human animal (MONDO:1013208) | | pancreatic adenocarcinoma, non-human animal (MONDO:1013310) | | complex vertebral malformation, elk (MONDO:7770234) | | congenital heart defect, blue-and-yellow macaw (MONDO:7770716) | | hyperoxaluria, koala (MONDO:7770620) | | difference of sexual development, mule (MONDO:7770340) | | central diabetes insipidus, non-human animal (MONDO:1013249) | | fibroblast growth factor 10 deficiency, Iberian ribbed newt (MONDO:7770510) | | eyelid neoplasm, non-human animal (MONDO:1013120) | | cholesteatoma, non-human animal (MONDO:1013713) | | humoral hypercalcemia of malignancy, non-human animal (MONDO:1013581) | | Stargardt disease, pig (MONDO:7770189) | | teratoma, non-human animal (MONDO:1013627) | | myelofibrosis, non-human animal (MONDO:1013597) | | hereditary myelopathy, dog (MONDO:7770485) | | rhizomelic chondrodysplasia punctata, GNPAT-related, cattle (MONDO:7770614) | | infertility, dog (MONDO:7770242) | | craniofacial dysplasia-hydrocephalus-dwarfism syndrome, cattle (MONDO:7770701) | | intestinal lymphangiectasia, non-human animal (MONDO:1013542) | | skin neoplasm, non-human animal (MONDO:1013150) | | spermatic cord torsion, non-human animal (MONDO:1013219) | | nasal cavity squamous cell carcinoma, non-human animal (MONDO:1013367) | | gastric adenocarcinoma, non-human animal (MONDO:1013271) | | inflammatory bowel disease, domestic cat (MONDO:7770068) | | bile duct neoplasm, non-human animal (MONDO:1013115) | | junctionalis epidermolysis bullosa, LAMB3-related, sheep (MONDO:7770587) | | chromosomal structural anomaly, translocation, centric fusion, horse (MONDO:7770723) | | obesity, macaque (MONDO:7770283) | | fatty metamorphosis of viscera, chicken (MONDO:7770284) | | third-degree atrioventricular block, non-human animal (MONDO:1013247) | | adenoviridae infectious disease, non-human animal (MONDO:1013488) | | TSEN2-related neurodevelopmental disorder with or without thrombotic microangiopathy (MONDO:1060216) | | inflammatory bowel disease, maned wolf (MONDO:7770418) | | tricuspid valve atresia, horse (MONDO:7770430) | | hypoxanthine guanine phosphoribosyltransferase deficiency, rabbit (MONDO:7770484) | | congenital myopathy 29 with contractures (MONDO:0981030) | | immunodeficiency, CARMIL2-related, dog (MONDO:7770448) | | adrenal cortex carcinoma, non-human animal (MONDO:1013301) | | dysgerminoma of ovary, non-human animal (MONDO:1013339) | | chromosomal abnormality, pig (MONDO:7770201) | | southern tick-associated rash illness (MONDO:1010205) | | primary adrenal insufficiency, non-human animal (MONDO:1013005) | | periodic fever syndrome, MTBP-related, dog (MONDO:1013792) | | eosinophilic granuloma, non-human animal (MONDO:1013053) | | xanthomatosis, yellow-footed rock-wallaby (MONDO:7770642) | | nasal cavity carcinoma, non-human animal (MONDO:1013282) | | XY difference of sexual development, cattle (MONDO:7770347) | | nasal dermoid cyst, non-human animal (MONDO:1013043) | | left ventricular noncompaction cardiomyopathy, Japanese macaque (MONDO:7770504) | | mesothelioma, non-human animal (MONDO:1013706) | | colitis, non-human animal (MONDO:1013646) | | skin angiosarcoma, non-human animal (MONDO:1013064) | | gout, non-human animal (MONDO:1013490) | | sacral agenesis, dog (MONDO:7770258) | | bladder carcinoma in situ, non-human animal (MONDO:1013300) | | carcinoma in situ of nasopharynx, non-human animal (MONDO:1013285) | | hypercholesterolaemia, LDLR-related, domestic cat (MONDO:7770634) | | pituitary gland adenoma, non-human animal (MONDO:1013318) | | choroid plexus carcinoma, non-human animal (MONDO:1013302) | | aspiration pneumonia, non-human animal (MONDO:1013186) | | polycystic ovary syndrome, non-human animal (MONDO:1013188) | | inflammatory bowel disease, rabbit (MONDO:7770465) | | penile neoplasm, non-human animal (MONDO:1013138) | | acute endometritis, non-human animal (MONDO:1013509) | | polyploidy, cattle (MONDO:7770683) | | sex chromosome difference of sexual development, mouflon (MONDO:7770688) | | hypogonadism, rln3b-related, Nile tilapia (MONDO:7770602) | | carcinoma of urethra, non-human animal (MONDO:1013297) | | obesity disorder, non-human animal (MONDO:1013600) | | spastic ataxia, SACS-related, dog (MONDO:7770350) | | thymoma type B3, non-human animal (MONDO:1013331) | | degenerative myelopathy, SP110-related, dog (MONDO:1013783) | | haplotype with homozygous deficiency JH1, zebu cattle (MONDO:7770384) | | pharynx cancer, non-human animal (MONDO:1013141) | | male subfertility, cheetah (MONDO:7770564) | | autosomal monosomy, cattle (MONDO:7770707) | | miosis, dog (MONDO:7770724) | | DND1-related reproductive disorder, striped catfish (MONDO:7770421) | | bronchial neoplasm, non-human animal (MONDO:1013522) | | pancytopenia, non-human animal (MONDO:1013603) | | polyglucosan body myopathy, RBCK1-related, dog (MONDO:7770655) | | primary melanoma of the central nervous system, non-human animal (MONDO:1013519) | | intestinal perforation, non-human animal (MONDO:1013393) | | glucagonoma, non-human animal (MONDO:1013630) | | sex chromosome difference of sexual development, cattle (MONDO:7770338) | | skin basal cell carcinoma, non-human animal (MONDO:1013332) | | rectum adenocarcinoma, non-human animal (MONDO:1013008) | | autosomal recessive hypertrophic cardiomyopathy, MYBPC3-related, domestic cat (MONDO:7770609) | | campylobacteriosis, non-human animal (MONDO:1013556) | | leg defects, horse (MONDO:7770462) | | disease by molecular mechanism, non-human animal (MONDO:7770017) | | vascular ectasia, non-human animal (MONDO:1013544) | | rectal neoplasm, non-human animal (MONDO:1013145) | | vaginitis, non-human animal (MONDO:1013625) | | atrial standstill, non-human animal (MONDO:1013263) | | cloaca, cattle (MONDO:7770385) | | aortic valve hypoplasia, cattle (MONDO:7770280) | | hemifacial microsomia, cattle (MONDO:7770704) | | myocarditis, non-human animal (MONDO:1013598) | | amelia, horse (MONDO:7770304) | | gastroenteritis, non-human animal (MONDO:1013577) | | myasthenia gravis, non-human animal (MONDO:1013103) | | dentinogenesis imperfecta, dog (MONDO:7770372) | | osteogenesis imperfecta, BMP1-related, domestic cat (MONDO:7770735) | | superficial keratitis, non-human animal (MONDO:1013085) | | liver lymphoma, non-human animal (MONDO:1013364) | | dental abnormalities, guinea pig (MONDO:7770631) | | hypertensive disorder, non-human animal (MONDO:1013079) | | Waldenström macroglobulinaemia, dog (MONDO:7770244) | | respiratory tract infectious disorder, non-human animal (MONDO:1013398) | | radiculopathy, non-human animal (MONDO:1013164) | | cardiac tamponade, non-human animal (MONDO:1013021) | | spondyloepiphyseal dysplasia tarda, medaka (MONDO:7770447) | | organophosphate poisoning, non-human animal (MONDO:1013082) | | cystic echinococcosis, non-human animal (MONDO:1013496) | | bronchiectasis, non-human animal (MONDO:1013555) | | invasive transitional cell carcinoma, MAP2K1-related, dog (MONDO:1013789) | | atresia intestinal, domestic cat (MONDO:7770404) | | ovarian disorder, non-human animal (MONDO:1013175) | | acute adrenal insufficiency, non-human animal (MONDO:1013006) | | junctionalis epidermolysis bullosa, COL17A1-related, domestic cat (MONDO:7770373) | | leukocyte adhesion deficiency, type I, zebu cattle (MONDO:7770382) | | common wart, non-human animal (MONDO:1013628) | | autosomal dominant progressive retinal atrophy, macaque (MONDO:7770287) | | tick paralysis, non-human animal (MONDO:1013224) | | cone degeneration, dog (MONDO:7770254) | | mitochondrial DNA depletion syndrome, Nile tilapia (MONDO:7770606) | | persistent frenulum praeputii, cheetah (MONDO:7770553) | | Crohn disease, non-human animal (MONDO:1013543) | | mycobacterial infectious disease, non-human animal (MONDO:1013104) | | viral meningitis, non-human animal (MONDO:1013520) | | ventricular tachycardia, non-human animal (MONDO:1013248) | | middle ear cholesterol granuloma, non-human animal (MONDO:1013476) | | oculocutaneous albinism, red-necked wallaby (MONDO:7770644) | | neutropenia, non-human animal (MONDO:1013629) | | frontal sinus squamous cell carcinoma, non-human animal (MONDO:1013366) | | sex chromosome monosomy, pig (MONDO:7770708) | | eosinophilic meningitis, non-human animal (MONDO:1013098) | | osteoma, non-human animal (MONDO:1013733) | | spinal cord neoplasm, non-human animal (MONDO:1013151) | | auditory-pigmentary syndrome, GRID1-related, cattle (MONDO:7770648) | | lameness, zebu cattle (MONDO:7770544) | | iritis, non-human animal (MONDO:1013626) | | balanoposthitis, non-human animal (MONDO:1013643) | | anterior segment dysgenesis, non-human animal (MONDO:1013470) | | pancreatic agenesis, macaque (MONDO:7770528) | | pleural neoplasm, non-human animal (MONDO:1013143) | | emphysematous cholecystitis, non-human animal (MONDO:1013546) | | lameness, goat (MONDO:7770217) | | primary systemic amyloidosis, non-human animal (MONDO:1013379) | | spondylosis, non-human animal (MONDO:1013214) | | hemopericardium, non-human animal (MONDO:1013579) | | Parkinson disease, medaka (MONDO:7770394) | | gallbladder adenocarcinoma, non-human animal (MONDO:1013307) | | rectum leiomyosarcoma, non-human animal (MONDO:1013353) | | chromosomal abnormality, common quail (MONDO:7770538) | | plasma cell myeloma, non-human animal (MONDO:1013329) | | spondylitis, non-human animal (MONDO:1013617) | | hypothyroidism, non-human animal (MONDO:1013584) | | external auditory canal atresia, domestic cat (MONDO:7770293) | | contagious pustular dermatitis, non-human animal (MONDO:1013483) | | invasive transitional cell carcinoma, NIPAL1-related, dog (MONDO:1013790) | | bone neoplasm, non-human animal (MONDO:1013116) | | spinocerebellar ataxia 52 (MONDO:0981162) | | chromosomal structural anomaly, translocation, centric fusion, brown trout (MONDO:7770680) | | pancreatic neoplasm, non-human animal (MONDO:1013136) | | dwarfism, ACAN-related, zebu cattle (MONDO:7770264) | | intestinal volvulus, pig (MONDO:7770624) | | dicrocoeliasis, non-human animal (MONDO:1013677) | | neurofibroma, non-human animal (MONDO:1013633) | | coloboma of iris, non-human animal (MONDO:1013480) | | gastric mucosal hypertrophy, non-human animal (MONDO:1013061) | | allergic urticaria, non-human animal (MONDO:1013078) | | orbit lymphoma, non-human animal (MONDO:1013095) | | nasolacrimal duct obstruction, llama (MONDO:7770474) | | difference of sexual development, rabbit (MONDO:7770368) | | stroke disorder, non-human animal (MONDO:1013025) | | congenital partial colonic agenesis, domestic cat (MONDO:7770351) | | corneal degeneration, non-human animal (MONDO:1013034) | | aortic valve stenosis, non-human animal (MONDO:1013014) | | brachygnathia, WNT10B-related, cattle (MONDO:7770307) | | oculocutaneous albinism, TYR-related, rhesus macaque (MONDO:7770289) | | cor triatriatum sinister, pig (MONDO:7770326) | | peroneal neuropathy, non-human animal (MONDO:1013436) | | medulloepithelioma, non-human animal (MONDO:1013704) | | claw/hoof disorders, goat (MONDO:7770218) | | persistent mullerian duct syndrome, AMHR2-related, dog (MONDO:7770328) | | fetal death, zebu cattle (MONDO:7770549) | | amelanotic melanoma, non-human animal (MONDO:1013406) | | neuritis, non-human animal (MONDO:1013181) | | botryomycosis, non-human animal (MONDO:1013755) | | autosomal dominant progressive retinal atrophy, pig (MONDO:7770408) | | mycetoma, non-human animal (MONDO:1013707) | | otitis externa, non-human animal (MONDO:1013171) | | anterior segment dysgenesis, domestic cat (MONDO:7770180) | | tricuspid valve prolapse, non-human animal (MONDO:1013228) | | brachycephaly, sheep (MONDO:7770733) | | lissencephaly, dog (MONDO:7770319) | | rhabdomyoma, non-human animal (MONDO:1013637) | | arthrogryposis, non-human animal (MONDO:1013642) | | sweat gland adenoma, non-human animal (MONDO:1013325) | | vitamin D-deficiency rickets, CYP2R1-related, domestic cat (MONDO:7770109) | | eastern equine encephalitis, non-human animal (MONDO:1013413) | | cone-rod dystrophy retinal atrophy, SPATA7-related, dog (MONDO:7770711) | | malignant mesothelioma, non-human animal (MONDO:1013266) | | selective IgM deficiency, non-human animal (MONDO:1013446) | | nodular episcleritis, non-human animal (MONDO:1013057) | | follicular thyroid adenoma, non-human animal (MONDO:1013326) | | uterine aplasia, alpaca (MONDO:7770428) | | bladder adenocarcinoma, non-human animal (MONDO:1013312) | | osteochondrodysplastic and cardiomyopathic syndrome, cattle (MONDO:7770533) | | rectum carcinoma in situ, non-human animal (MONDO:1013279) | | tibial neuropathy, non-human animal (MONDO:1013437) | | aflatoxicosis, non-human animal (MONDO:1013683) | | lymphatic system disorder, non-human animal (MONDO:1013777) | | pharyngitis, non-human animal (MONDO:1013607) | | glycogen storage disease due to glycogen branching enzyme deficiency, non-human animal (MONDO:1013511) | | vestibular disease, goat (MONDO:7770744) | | bicipital tenosynovitis, non-human animal (MONDO:1013401) | | salivary gland carcinoma, non-human animal (MONDO:1013291) | | developmental dysplasia of the hip, non-human animal (MONDO:1013075) | | glucose-6-phosphate dehydrogenase deficiency, dog (MONDO:7770486) | | nasolacrimal duct obstruction, alpaca (MONDO:7770473) | | anhidrosis, horse (MONDO:7770577) | | complex vertebral malformation, dog (MONDO:7770400) | | papillomatosis, non-human animal (MONDO:1013658) | | difference of sexual development, wolf (MONDO:7770429) | | uveodermatological syndrome, dog (MONDO:7770363) | | chromosomal abnormality, donkey (MONDO:7770491) | | scrotal disorder, non-human animal (MONDO:1013256) | | chronic lymphocytic leukemia, mule (MONDO:7770219) | | pulmonary edema, non-human animal (MONDO:1013199) | | periodontal disorder, non-human animal (MONDO:1013185) | | leopard complex spotting coat colour, TRPM1-related, horse (MONDO:7770096) | | vulva cancer, non-human animal (MONDO:1013163) | | Rett syndrome, rhesus macaque (MONDO:7770183) | | Rotavirus infection, non-human animal (MONDO:1013380) | | oral cavity neoplasm, non-human animal (MONDO:1013133) | | amelia, cattle (MONDO:7770388) | | vestibular ataxia, non-human animal (MONDO:1013471) | | cerebellar abiotrophy, TOE1-related, horse (MONDO:1013781) | | congenital stationary night blindness, non-human animal (MONDO:1013411) | | intestinal impaction, non-human animal (MONDO:1013420) | | short tail sperm, pig (MONDO:7770051) | | sex chromosome difference of sexual development, horse (MONDO:7770337) | | renal adenoma, non-human animal (MONDO:1013320) | | rectal prolapse, non-human animal (MONDO:1013202) | | lens luxation, Huon tree kangaroo (MONDO:7770643) | | gastric leiomyoma, non-human animal (MONDO:1013347) | | lactic acidosis, non-human animal (MONDO:1013514) | | combined lipase deficiency, LMF1-related, horse (MONDO:7770641) | | luteoma of pregnancy, non-human animal (MONDO:1013632) | | cold agglutinin disease, non-human animal (MONDO:1013029) | | esophageal adenocarcinoma, non-human animal (MONDO:1013007) | | appendicitis, non-human animal (MONDO:1013684) | | progressive retinal atrophy, CNGB1-related, dog (MONDO:7770261) | | amorphus globosus, horse (MONDO:7770392) | | methylmalonic-coA mutase deficiency, MMUT-related, sheep (MONDO:7770469) | | carcinoid tumor, non-human animal (MONDO:1013725) | | chondroma, non-human animal (MONDO:1013726) | | agenesis of corpus callosum, sheep (MONDO:7770598) | | XY difference of sexual development, goat (MONDO:7770583) | | macrocephaly, macaque (MONDO:7770202) | | pituitary cancer, non-human animal (MONDO:1013142) | | myopathy, 'dozer lamb syndrome', sheep (MONDO:7770567) | | tongue disorder, non-human animal (MONDO:1013402) | | spinal cord disorder, non-human animal (MONDO:1013400) | | uterine aplasia, domestic cat (MONDO:7770426) | | male subfertility, cattle (MONDO:7770536) | | Woodhouse-Sakati syndrome, Dcaf17-related, golden hamster (MONDO:7770525) | | uterine aplasia, cattle (MONDO:7770424) | | gingival neoplasm, non-human animal (MONDO:1013252) | | curly coat, KRT25-related, horse (MONDO:7770729) | | podocytopathy (MONDO:0700328) | | cystic microphthalmia, horse (MONDO:7770558) | | albinism coat color, New Zealand fur seal (MONDO:7770712) | | gastric squamous cell carcinoma, non-human animal (MONDO:1013456) | | polyp of rectum, non-human animal (MONDO:1013193) | | translocation chromosomal structural anomaly, dog (MONDO:7770661) | | vesiculitis, non-human animal (MONDO:1013447) | | toxic epidermal necrolysis, non-human animal (MONDO:1013225) | | isolated thyrotropin-releasing hormone deficiency, non-human animal (MONDO:1013513) | | ulnar neuropathy, non-human animal (MONDO:1013184) | | dilated cardiomyopathy, ABCC9-related, dog (MONDO:7770247) | | sex chromosome difference of sexual development, pig (MONDO:7770344) | | disorder of ear, non-human animal (MONDO:1013049) | | ear infection, non-human animal (MONDO:1013050) | | crest, mallard (MONDO:7770310) | | autoimmune lymphoproliferative syndrome, dog (MONDO:7770737) | | cutaneous mucinosis, non-human animal (MONDO:1013595) | | Arenaviridae infectious disease, non-human animal (MONDO:1013489) | | degenerative myelopathy, SOD1-related, dog (MONDO:1013782) | | second-degree atrioventricular block, non-human animal (MONDO:1013246) | | tetanus, non-human animal (MONDO:1013620) | | Mycoplasmoides infection, non-human animal (MONDO:1013425) | | chromosomal structural anomaly, translocation, centric fusion, raccoon dog (MONDO:7770672) | | arachnomelia, cattle (MONDO:7770700) | | thrombotic disease, non-human animal (MONDO:1013222) | | femoral neuropathy, non-human animal (MONDO:1013434) | | thymoma, non-human animal (MONDO:1013724) | | chronic kidney disease, non-human animal (MONDO:1013261) | | liver failure, non-human animal (MONDO:1013775) | | inflammation and necrosis syndrome, pig (MONDO:7770187) | | urethra adenocarcinoma, non-human animal (MONDO:1013311) | | patched1-related cardiovascular disorder, Nile tilapia (MONDO:7770601) | | perinatal lethality, EGFR-related, cattle (MONDO:7770726) | | splenic abscess, non-human animal (MONDO:1013001) | | uterine carcinoma, non-human animal (MONDO:1013305) | | phimosis, non-human animal (MONDO:1013660) | | tracheal disorder, non-human animal (MONDO:1013403) | | nutritional biotin deficiency, non-human animal (MONDO:1013493) | | fibroma, non-human animal (MONDO:1013698) | | tumor lysis syndrome, non-human animal (MONDO:1013230) | | obesity, sheep (MONDO:7770596) | | skeletal deformity, Atlantic salmon (MONDO:7770548) | | urethra transitional cell carcinoma, non-human animal (MONDO:1013370) | | fragile X syndrome, chicken (MONDO:7770167) | | impetigo, non-human animal (MONDO:1013668) | | lissencephaly, ferret (MONDO:7770523) | | polyradiculoneuropathy, non-human animal (MONDO:1013609) | | pure red-cell aplasia, non-human animal (MONDO:1013201) | | chromosomal structural anomaly, translocation, centric fusion, rabbit (MONDO:7770674) | | primordial disproportionate dwarfism with craniofacial dysmorphism, PDGFRA-related, cattle (MONDO:7770695) | | adenoma of small intestine, non-human animal (MONDO:1013322) | | diffuse cutaneous mucinosis, non-human animal (MONDO:1013101) | | nasopharyngeal carcinoma, non-human animal (MONDO:1013284) | | benign muscle neoplasm, non-human animal (MONDO:1013130) | | meningitis, non-human animal (MONDO:1013763) | | skeletal abnormality, silver carp (MONDO:7770603) | | synostosis, non-human animal (MONDO:1013618) | | balanitis, non-human animal (MONDO:1013551) | | laryngeal neoplasm, non-human animal (MONDO:1013126) | | stomach carcinoma in situ, non-human animal (MONDO:1013294) | | enterocolitis, non-human animal (MONDO:1013759) | | metabolic acidosis, non-human animal (MONDO:1013265) | | aspiration pneumonia, dog (MONDO:7770082) | | transmission ratio distortion, horse (MONDO:7770297) | | paronychia, non-human animal (MONDO:1013606) | | difference of sexual development, tongue sole (MONDO:7770332) | | primary bone lymphoma, non-human animal (MONDO:1013362) | | diclofenac toxicity (MONDO:7770396) | | spinal injury, non-human animal (MONDO:1013382) | | intestinal infectious disease, non-human animal (MONDO:1013541) | | hemifacial microsomia, LAMB1-related, cattle (MONDO:7770149) | | portal vein thrombosis, non-human animal (MONDO:1013221) | | ciliopathy, chicken (MONDO:7770556) | | XY difference of sexual development, HSD17B3-related, dog (MONDO:7770330) | | macrostomus, rhesus macaque (MONDO:7770058) | | kidney failure, non-human animal (MONDO:1013779) | | vascular myelopathy, non-human animal (MONDO:1013210) | | molluscum contagiosum, non-human animal (MONDO:1013521) | | keratopathy, non-human animal (MONDO:1013703) | | sebaceous gland neoplasm, non-human animal (MONDO:1013149) | | auditory-pigmentary syndrome, PAX3-related, domestic cat (MONDO:7770415) | | common cold, non-human animal (MONDO:1013207) | | conjunctival tumor, non-human animal (MONDO:1013119) | | deafness, LHFPL5-related, domestic cat (MONDO:7770721) | | anhidrosis, non-human animal (MONDO:1013641) | | endophthalmitis, non-human animal (MONDO:1013575) | | anophthalmia/microphthalmia, gja8b-related, Mexican tetra (MONDO:7770613) | | frontotemporal dementia and/or amyotrophic lateral sclerosis 1, macaque (MONDO:7770263) | | polyploidy, pig (MONDO:7770685) | | neuronal ceroid lipofuscinosis, TPP1-related, macaque (MONDO:7770197) | | ear neoplasm, non-human animal (MONDO:1013113) | | septic peritonitis, non-human animal (MONDO:1013440) | | lathyrism, non-human animal (MONDO:1013655) | | tricuspid valve dysplasia, ferret (MONDO:7770545) | | ichthyosis, ALOXE3-related, dog (MONDO:7770692) | | leg weakness, chicken (MONDO:7770518) | | oculocutaneous albinism, TYR-related, axolotl (MONDO:7770111) | | atrioventricular block, non-human animal (MONDO:1013384) | | eosinophilic colitis, non-human animal (MONDO:1013030) | | aspergillosis, non-human animal (MONDO:1013550) | | chromosomal abnormality, Barbary partridge (MONDO:7770542) | | ulcerative colitis, non-human animal (MONDO:1013031) | | spinal cord ependymoma, non-human animal (MONDO:1013250) | | dermatitis, non-human animal (MONDO:1013739) | | gastritis, non-human animal (MONDO:1013744) | | neurolymphomatosis, non-human animal (MONDO:1013502) | | meningioma, dog (MONDO:7770179) | | constrictive pericarditis, non-human animal (MONDO:1013433) | | lung abscess, non-human animal (MONDO:1013264) | | haemophilus infectious disease, non-human animal (MONDO:1013497) | | bone marrow disorder, non-human animal (MONDO:1013016) | | tracheitis, non-human animal (MONDO:1013623) | | corticosteroid myopathy, non-human animal (MONDO:1013108) | | cholecystitis, non-human animal (MONDO:1013562) | | exocrine pancreatic carcinoma, non-human animal (MONDO:1013288) | | rhinitis, non-human animal (MONDO:1013749) | | cerebellar disorder, non-human animal (MONDO:1013387) | | acute lymphoblastic leukemia, non-human animal (MONDO:1013088) | | neuronal ceroid lipofuscinosis, 7, MFSD8-related, rabbit (MONDO:7770481) | | corneal edema, non-human animal (MONDO:1013506) | | XY difference of sexual development, wood lemming (MONDO:7770681) | | blindness (disorder), non-human animal (MONDO:1013737) | | ichthyosis, ABCA12-related, domestic cat (MONDO:7770720) | | chromosomal structural anomaly, translocation, centric fusion, Arabian oryx (MONDO:7770669) | | RAD50 double-stranded break point repair protein deficiency, medaka (MONDO:7770215) | | dry eye syndrome, non-human animal (MONDO:1013086) | | acute lung injury, non-human animal (MONDO:1013003) | | myocardial infarction, non-human animal (MONDO:1013106) | | mucopolysaccharidosis I, Japanese macaque (MONDO:7770590) | | renal tubular acidosis, non-human animal (MONDO:1013532) | | parathyroid gland carcinoma, non-human animal (MONDO:1013137) | | pneumococcal infection, non-human animal (MONDO:1013505) |

</details>

<details> <summary>Nodes renamed: 236</summary>

| ID | Old Label | New Label | ----|----|----| | MONDO:1011205 | Van den Ende-Gupta syndrome, dog | Van den Ende-Gupta syndrome, SCARF2-related, dog | | MONDO:1011286 | Leber hereditary optic neuropathy, cattle | Leber hereditary optic neuropathy, ND4L-related, cattle | | MONDO:1010925 | muscular dystrophy, Duchenne type, pig | muscular dystrophy, Duchenne type, DMD-related, pig | | MONDO:1012147 | malignant hyperthermia, horse | malignant hyperthermia, RYR1-related, horse | | MONDO:1010447 | dilated cardiomyopathy, turkey | dilated cardiomyopathy, TNNT2-related, turkey | | MONDO:1011597 | severe combined immunodeficiency disease, horse | severe combined immunodeficiency disease, PRKDC-related, horse | | MONDO:1010701 | pyruvate kinase deficiency of erythrocyte, dog | pyruvate kinase deficiency of erythrocyte, PKLR-related, dog | | MONDO:1010668 | factor XIII deficiency, cattle | factor XIII deficiency, F13A1-related, cattle | | MONDO:1011435 | Becker type muscular dystrophy, non-human animal | Becker type muscular dystrophy, non-human animal, DMD-related, domestic cat | | MONDO:1012170 | lower motor neuron disease, sheep | lower motor neuron disease, AGTPBP1-related, sheep | | MONDO:1010713 | pyruvate dehydrogenase deficiency, dog | pyruvate dehydrogenase deficiency, PDP1-related, dog | | MONDO:1010588 | familial goiter, cattle | familial goiter, TG-related, cattle | | MONDO:0019835 | primary hypophysitis | lymphocytic hypophysitis | | MONDO:1012383 | trapped neutrophil syndrome, dog | trapped neutrophil syndrome, VPS13B-related, dog | | MONDO:1011057 | polycystic kidney disease, pig | polycystic kidney disease, PKD1-related, pig | | MONDO:1012484 | hoof wall separation syndrome, horse | hoof wall separation syndrome, SERPINB11-related, horse | | MONDO:1012326 | premature senesence, rabbit | premature senesence, LMNA-related, rabbit | | MONDO:1012124 | hypotrophic axonopathy, Japanese quail | hypotrophic axonopathy, NEFL-related, Japanese quail | | MONDO:1010696 | analphalipoproteinaemia, chicken | analphalipoproteinaemia, ABCA1-related, chicken | | MONDO:1010418 | narcolepsy, dog | narcolepsy, HCRTR2-related, dog | | MONDO:1010791 | tricho-dento-osseous-like syndrome, cattle | tricho-dento-osseous-like syndrome, DLX3-related, cattle | | MONDO:1012414 | pulmonary hypoplasia with anasarca, cattle | pulmonary hypoplasia with anasarca, ADAMTS3-related, cattle | | MONDO:1012407 | acral mutilation syndrome, dog | acral mutilation syndrome, GDNF-related, dog | | MONDO:1011280 | microphthalmia, isolated, with coloboma, dog | microphthalmia, isolated, with coloboma, RBP4-related, dog | | MONDO:1011556 | medium-chain acyl-CoA dehydrogenase deficiency, dog | medium-chain acyl-CoA dehydrogenase deficiency, ACADM-related, dog | | MONDO:1010759 | acrodermatitis enteropathica, cattle | acrodermatitis enteropathica, SLC39A4-related, cattle | | MONDO:1011498 | enteropathy-associated T cell lymphoma, domestic cat | enteropathy-associated T cell lymphoma, STAT5B-related, domestic cat | | MONDO:1011078 | urolithiasis, dog | urolithiasis, SLC2A9-related, dog | | MONDO:1010928 | congenital pseudomyotonia, cattle | congenital pseudomyotonia, ATP2A1-related, cattle | | MONDO:1010854 | Krabbe disease, Rhesus monkey | Krabbe disease, GALC-related, Rhesus macaque | | MONDO:1012362 | photoreceptor dysplasia, dog | photoreceptor dysplasia, PPT1-related, dog | | MONDO:1011014 | Alexander disease, dog | Alexander disease, GFAP-related, dog | | MONDO:1010636 | factor XI deficiency, dog | factor XI deficiency, F11-related, dog | | MONDO:1012513 | verrucous epidermal keratinocytic nevi, dog | verrucous epidermal keratinocytic nevi, NSDHL-related, dog | | MONDO:1012359 | progressive rod-cone degeneration, dog | progressive rod-cone degeneration, PRCD-related, dog | | MONDO:1011522 | hemophilia A, domestic cat | hemophilia A, F8-related, domestic cat | | MONDO:1011090 | renal dysplasia, cattle | renal dysplasia, CLDN16-related, cattle | | MONDO:1012506 | degenerative encephalopathy, dog | degenerative encephalopathy, RB1CC1-related, dog | | MONDO:1012529 | recurrent inflammatory pulmonary disease, dog | recurrent inflammatory pulmonary disease, AKNA-related, dog | | MONDO:1012384 | forelimb-girdle muscular anomaly, cattle | forelimb-girdle muscular anomaly, GFRA1-related, cattle | | MONDO:1010865 | alpha-mannosidosis, cattle | alpha-mannosidosis, MAN2B1-related, cattle | | MONDO:1012070 | dystrophic epidermolysis bullosa, cattle | dystrophic epidermolysis bullosa, COL7A1-related, cattle | | MONDO:1011242 | microphthalmia, sheep | microphthalmia, PITX3-related, sheep | | MONDO:1010521 | mandibulofacial dysostosis, cattle | mandibulofacial dysostosis, CYP26C1-related, cattle | | MONDO:1010833 | Wilson disease, domestic cat | Wilson disease, ATP7B-related, domestic cat | | MONDO:1010657 | prekallikrein deficiency, dog | prekallikrein deficiency, KLKB1-related, dog | | MONDO:1010545 | cystic fibrosis, sheep | cystic fibrosis, CFTR-related, sheep | | MONDO:1011495 | Ehlers-Danlos syndrome, horse | Ehlers-Danlos syndrome, PPIB-related, horse | | MONDO:1012312 | congenital erythropoietic porphyria, domestic cat | congenital erythropoietic porphyria, UROS-related, domestic cat | | MONDO:1012400 | dilute coat color with neurological defects, dog | dilute coat color with neurological defects, MYO5A-related, dog | | MONDO:1010723 | glucocorticoid resistance, dog | glucocorticoid resistance, NR3C1-related, dog | | MONDO:1010777 | atrichia with papular lesions, Rhesus monkey | atrichia with papular lesions, Rhesus monkey, HR-related, rhesus macaque | | MONDO:0011996 | chronic myelogenous leukemia, BCR-ABL1 positive | chronic myeloid leukemia | | MONDO:1012520 | bilateral deafness and vestibular dysfunction, dog | bilateral deafness and vestibular dysfunction, MYO7A-related, dog | | MONDO:1010831 | tetradysmelia, cattle | tetradysmelia, RSPO2-related, cattle | | MONDO:1012341 | spinal dysmyelination, cattle | spinal dysmyelination, SPAST-related, cattle | | MONDO:1012145 | malignant hyperthermia, dog | malignant hyperthermia, RYR1-related, dog | | MONDO:1010929 | myotubular myopathy 1, dog | myotubular myopathy, MTM1-related, dog | | MONDO:1012419 | episodic falling, dog | episodic falling, BCAN-related, dog | | MONDO:1012035 | cardiomyopathy and woolly haircoat syndrome, cattle | cardiomyopathy and woolly haircoat syndrome, PPP1R13L-related, cattle | | MONDO:1012065 | autosomal dwarfism, chicken | autosomal dwarfism, TMEM263-related, chicken | | MONDO:1011487 | complement component 3 deficiency, dog | complement component 3 deficiency, C3-related, dog | | MONDO:1012432 | congenital keratoconjunctivitis sicca and ichthyosiform dermatosis, dog | congenital keratoconjunctivitis sicca and ichthyosiform dermatosis, FAM83H-related, dog | | MONDO:0008549 | thoracic dysostosis, isolated | obsolete thoracic dysostosis, isolated | | MONDO:1012398 | segmental axonopathy, sheep | segmental axonopathy, ALS2-related, sheep | | MONDO:1012514 | verrucous epidermal keratinocytic nevi, domestic cat | verrucous epidermal keratinocytic nevi, NSDHL-related, domestic cat | | MONDO:1010855 | Krabbe disease, dog | Krabbe disease, GALC-related, dog | | MONDO:1012178 | myoclonus epilepsy of Lafora, dog | myoclonus epilepsy of Lafora, NHLRC1-related, dog | | MONDO:1011178 | osteopetrosis, Japanese quail | osteopetrosis, MITF-related, Japanese quail | | MONDO:1010758 | acrodermatitis enteropathica, domestic cat | acrodermatitis enteropathica, SLC39A4-related, domestic cat | | MONDO:1010644 | hemophilia B, domestic cat | hemophilia B, F9-related, domestic cat | | MONDO:1010536 | megacolon, horse | megacolon, EDNRB-related, horse | | MONDO:1012490 | vertebral and spinal dysplasia, cattle | vertebral and spinal dysplasia, TBXT-related, cattle | | MONDO:1010718 | dihydropyrimidinase deficiency, domestic cat | dihydropyrimidinase deficiency, DPYS-related, domestic cat | | MONDO:1012569 | hepatocellular fibrinogen storage disease, cattle | hepatocellular fibrinogen storage disease, DGKG-related, cattle | | MONDO:1010923 | muscular dystrophy, Duchenne type, dog | muscular dystrophy, Duchenne type, DMD-related, dog | | MONDO:1010632 | factor VII deficiency, dog | factor VII deficiency, F7-related, dog | | MONDO:1011054 | polycystic kidney disease, domestic cat | polycystic kidney disease, PKD1-related, domestic cat | | MONDO:1010905 | deficiency of uridine monophosphate synthase, cattle | deficiency of uridine monophosphate synthase, UMPS-related, cattle | | MONDO:1010451 | dilated cardiomyopathy, cattle | dilated cardiomyopathy, OPA3-related, cattle | | MONDO:1012535 | cardiomyopathy and juvenile mortality, dog | cardiomyopathy and juvenile mortality, YARS2-related, dog | | MONDO:1011207 | hypophosphatasia, dog | hypophosphatasia, ALPL-related, dog | | MONDO:1012266 | androgen insensitivity syndrome, horse | androgen insensitivity syndrome, AR-related, horse | | MONDO:1010643 | hemophilia B, dog | hemophilia B, F9-related, dog | | MONDO:1010829 | tibial hemimelia, cattle | tibial hemimelia, ALX4-related, cattle | | MONDO:1010909 | muscular dystrophy, chicken | muscular dystrophy, WWP1-related, chicken | | MONDO:1010863 | alpha-mannosidosis, domestic guinea pig | alpha-mannosidosis, domestic guinea pig, Man2b1-related, guinea pig | | MONDO:1012363 | myopathy of the diaphragmatic muscles, cattle | myopathy of the diaphragmatic muscles, HSPA1A-related, cattle | | MONDO:1012271 | thrombasthenia, domestic cat | thrombasthenia, ITGA2B-related, domestic cat | | MONDO:1012518 | immune-mediated myositis, horse | immune-mediated myositis, MYH1-related, horse | | MONDO:1010638 | factor XI deficiency, cattle | factor XI deficiency, F11-related, cattle | | MONDO:1010520 | cleft lip with or without cleft palate, dog | cleft lip with or without cleft palate, ADAMTS20-related, dog | | MONDO:1012511 | generalized myoclonic epilepsy with photosensitivity, dog | generalized myoclonic epilepsy with photosensitivity, DIRAS1-related, dog | | MONDO:1011519 | hemophilia A, cattle | hemophilia A, F8-related, cattle | | MONDO:1012422 | exfoliative cutaneous lupus erythematosus, dog | exfoliative cutaneous lupus erythematosus, UNC93B1-related, dog | | MONDO:1011018 | L-2-hydroxyglutaricacidemia, dog | L-2-hydroxyglutaricacidemia, L2HGDH-related, dog | | MONDO:1012148 | malignant hyperthermia, pig | malignant hyperthermia, RYR1-related, pig | | MONDO:1012528 | unilateral deafness and vestibular dysfunction, dog | unilateral deafness and vestibular dysfunction, PTPRQ-related, dog | | MONDO:1012408 | colorectal hamartomatous polyposis and ganglioneuromatosis, dog | colorectal hamartomatous polyposis and ganglioneuromatosis, PTEN-related, dog | | MONDO:1012522 | turning calves syndrome, cattle | turning calves syndrome, SLC25A46-related, cattle | | MONDO:1010445 | dilated cardiomyopathy, golden hamster | dilated cardiomyopathy, SGCD-related, golden hamster | | MONDO:1010564 | congenital adrenal hyperplasia, rabbit | congenital adrenal hyperplasia, CYP11A1-related, rabbit | | MONDO:1011156 | Marfan syndrome, cattle | Marfan syndrome, FBN1-related, cattle | | MONDO:1010762 | protoporphyria, cattle | protoporphyria, FECH-related, cattle | | MONDO:1012519 | lethal acrodermatitis, dog | lethal acrodermatitis, MKLN1-related, dog | | MONDO:1012348 | recessive hypotrichosis, dog | recessive hypotrichosis, SGK3-related, dog | | MONDO:1012444 | polled and multisystemic syndrome, cattle | polled and multisystemic syndrome, ZEB2-related, cattle | | MONDO:1011502 | Fanconi syndrome, cattle | Fanconi syndrome, SLC2A2-related, cattle | | MONDO:1011031 | succinic semialdehyde dehydrogenase deficiency, dog | succinic semialdehyde dehydrogenase deficiency, ALDH5A1-related, dog | | MONDO:0034186 | autosomal recessive extra-oral halitosis | obsolete autosomal recessive extra-oral halitosis | | MONDO:1012403 | contractural arachnodactyly, cattle | contractural arachnodactyly, ADAMTSL3-related, cattle | | MONDO:1010637 | factor XI deficiency, domestic cat | factor XI deficiency, F11-related, domestic cat | | MONDO:1010417 | myoclonus, cattle | myoclonus, GLRA1-related, cattle | | MONDO:1011554 | ligneous membranitis, dog | ligneous membranitis, PLG-related, dog | | MONDO:1012510 | facial dysplasia syndrome, cattle | facial dysplasia syndrome, FGFR2-related, cattle | | MONDO:1012441 | familial episodic spinocerebellar ataxia, sheep | familial episodic spinocerebellar ataxia, FGF14-related, sheep | | MONDO:1012564 | growth and respiratory lethal syndrome, cattle | growth and respiratory lethal syndrome, EDN2-related, cattle | | MONDO:1012433 | proportionate dwarfism with inflammatory lesions, cattle | proportionate dwarfism with inflammatory lesions, RNF11-related, cattle | | MONDO:1010409 | epilepsy, chicken | epilepsy, LOC430486-related, chicken | | MONDO:1012525 | Meckel-like hepatorenal fibrocystic dysplasia syndrome, sheep | Meckel-like hepatorenal fibrocystic dysplasia syndrome, TMEM67-related, sheep | | MONDO:1010827 | syndactyly, cattle | syndactyly, LRP4-related, cattle | | MONDO:1010809 | polydactyly, chicken | polydactyly, SHH-related, chicken | | MONDO:1010741 | autoimmune lymphoproliferative syndrome, domestic cat | autoimmune lymphoproliferative syndrome, FASLG-related, domestic cat | | MONDO:1010697 | citrullinaemia, cattle | citrullinaemia, ASS1-related, cattle | | MONDO:1010631 | Chediak-Higashi syndrome, cattle | Chediak-Higashi syndrome, LYST-related, cattle | | MONDO:1011536 | hyperkalemic periodic paralysis, horse | hyperkalemic periodic paralysis, SCN4A-related, horse | | MONDO:1012051 | Collie eye anomaly, dog | Collie eye anomaly, NHEJ1-related, dog | | MONDO:1012389 | exercise-induced collapse, dog | exercise-induced collapse, DNM1-related, dog | | MONDO:1012272 | thrombasthenia, horse | thrombasthenia, ITGA2B-related, horse | | MONDO:1010702 | pyruvate kinase deficiency of erythrocyte, domestic cat | pyruvate kinase deficiency of erythrocyte, PKLR-related, domestic cat | | MONDO:1012492 | neurodegenerative vacuolar storage disease, dog | neurodegenerative vacuolar storage disease, ATG4D-related, dog | | MONDO:1012491 | lethal arthrogryposis syndrome, cattle | lethal arthrogryposis syndrome, PIGH-related, cattle | | MONDO:1012394 | growth-hormone deficiency dwarfism, zebu cattle | growth-hormone deficiency dwarfism, LOC109574543-related, zebu cattle | | MONDO:1012512 | naked foal syndrome, horse | naked foal syndrome, ST14-related, horse | | MONDO:1012466 | perinatal weak calf syndrome, cattle | perinatal weak calf syndrome, IARS-related, cattle | | MONDO:1011480 | Becker type muscular dystrophy, pig | Becker type muscular dystrophy, DMD-related, pig | | MONDO:1010669 | myeloperoxidase deficiency, dog | myeloperoxidase deficiency, MPO-related, dog | | MONDO:1012259 | spinal dysraphism, dog | spinal dysraphism, NKX2-8-related, dog | | MONDO:1011201 | schmid metaphyseal chondrodysplasia dwarfism, pig | schmid metaphyseal chondrodysplasia dwarfism, COL10A1-related, pig | | MONDO:1012292 | subacute necrotising encephalopathy of Leigh, dog | subacute necrotising encephalopathy of Leigh, SLC19A3-related, dog | | MONDO:1012536 | atypical thrombasthenia, horse | atypical thrombasthenia, SEL1L-related, horse | | MONDO:1011022 | lissencephaly and cerebellar hypoplasia, dog | lissencephaly and cerebellar hypoplasia, RELN-related, dog | | MONDO:1010629 | Chediak-Higashi syndrome, domestic cat | Chediak-Higashi syndrome, LYST-related, domestic cat | | MONDO:1012392 | neonatal encephalopathy with seizures, dog | neonatal encephalopathy with seizures, ATF2-related, dog | | MONDO:1012573 | pyknodysostosis, domestic cat | pyknodysostosis, CTSK-related, domestic cat | | MONDO:1012358 | early retinal degeneration, dog | early retinal degeneration, STK38L-related, dog | | MONDO:1011204 | spondylocostal dysostosis, autosomal recessive, dog | spondylocostal dysostosis, autosomal recessive, HES7-related, dog | | MONDO:1011020 | hyperekplexia, dog | hyperekplexia, SLC6A5-related, dog | | MONDO:1011026 | lissencephaly and cerebellar hypoplasia, sheep | lissencephaly and cerebellar hypoplasia, RELN-related, sheep | | MONDO:1010640 | factor XII deficiency, domestic cat | factor XII deficiency, F12-related, domestic cat | | MONDO:1012440 | lethal multi-organ developmental dysplasia, cattle | lethal multi-organ developmental dysplasia, KDM2B-related, cattle | | MONDO:0700161 | canine gastrointestinal stromal tumor | canine gastrointestinal stromal tumor, KIT-related, dog | | MONDO:1012521 | bilateral deafness and vestibular dysfunction, pig | bilateral deafness and vestibular dysfunction, MYO7A-related, pig | | MONDO:1012449 | squamous cell carcinoma of the digit, dog | squamous cell carcinoma of the digit, KITLG-related, dog | | MONDO:1060194 | FAS-related autoimmune lymphoproliferative syndrome | FAS-related autoimmune lymphoproliferative immune disorder | | MONDO:1012524 | diffuse cystic renal dysplasia and hepatic fibrosis, dog | diffuse cystic renal dysplasia and hepatic fibrosis, INPP5E-related, dog | | MONDO:1012489 | hypotrichosis with short life expectancy, domestic cat | hypotrichosis with short life expectancy, FOXN1-related, domestic cat | | MONDO:1012487 | zinc deficiency-like syndrome, cattle | zinc deficiency-like syndrome, PLD4-related, cattle | | MONDO:1012325 | premature senesence, pig | premature senesence, LMNA-related, pig | | MONDO:1012320 | high-frequency tremor, pig | high-frequency tremor, MYH7-related, pig | | MONDO:1011483 | beta-mannosidosis, goat | beta-mannosidosis, MANBA-related, goat | | MONDO:1011525 | hemophilia A, sheep | hemophilia A, F8-related, sheep | | MONDO:1012344 | familial convulsions and ataxia, cattle | familial convulsions and ataxia, CACNA1A-related, cattle | | MONDO:1010930 | myotubular myopathy 1, domestic cat | myotubular myopathy, MTM1-related, domestic cat | | MONDO:1010988 | hydrocephalus, horse | hydrocephalus, B3GALNT2-related, horse | | MONDO:1010614 | congenital adrenal hyperplasia due to 11-beta hydroxylase deficiency, domestic cat | congenital adrenal hyperplasia due to 11-beta hydroxylase deficiency, CYP11B1-related, domestic cat | | MONDO:1011482 | beta-mannosidosis, dog | beta-mannosidosis, MANBA-related, dog | | MONDO:1012373 | retinal dysplasia and degeneration, chicken | retinal dysplasia and degeneration, MPDZ-related, chicken | | MONDO:1012295 | axonopathy, cattle | axonopathy, MFN2-related, cattle | | MONDO:1012494 | autosomal T cell-negative, B cell-negative, NK cell-positive severe combined immunodeficiency disease with sensitivity to ionizing radiation, pig | autosomal T cell-negative, B cell-negative, NK cell-positive severe combined immunodeficiency disease, DCLRE1C-related, pig | | MONDO:1012409 | gallbladder mucocele, dog | gallbladder mucocele, ABCB4-related, dog | | MONDO:1012270 | thrombasthenia, dog | thrombasthenia, ITGA2B-related, dog | | MONDO:1010710 | trimethylaminuria (fishy taint), chicken | trimethylaminuria (fishy taint), FMO3-related, chicken | | MONDO:1010712 | trimethylaminuria (fishy taint), cattle | trimethylaminuria (fishy taint), FMO3-related, cattle | | MONDO:0030983 | Waardenburg syndrome, IIa 2F | Waardenburg syndrome 2F | | MONDO:1011278 | macular corneal dystrophy, dog | macular corneal dystrophy, LOC489707-related, dog | | MONDO:1012377 | nasal parakeratosis, dog | nasal parakeratosis, SUV39H2-related, dog | | MONDO:1012068 | dystrophic epidermolysis bullosa, dog | dystrophic epidermolysis bullosa, COL7A1-related, dog | | MONDO:1012561 | mitochondrial fission encephalopathy, dog | mitochondrial fission encephalopathy, MFF-related, dog | | MONDO:1011521 | hemophilia A, dog | hemophilia A, F8-related, dog | | MONDO:1011203 | osteopetrosis with gingival hamartomas, cattle | osteopetrosis with gingival hamartomas, CLCN7-related, cattle | | MONDO:1010849 | glycogen storage disease II, Japanese quail | glycogen storage disease, GAA-related, Japanese quail | | MONDO:1011208 | hypophosphatasia, sheep | hypophosphatasia, ALPL-related, sheep | | MONDO:1012478 | upper airway syndrome, dog | upper airway syndrome, ADAMTS3-related, dog | | MONDO:1010832 | Wilson disease, dog | Wilson disease, ATP7B-related, dog | | MONDO:1012565 | dyserythropoietic anemia and myopathy syndrome, dog | dyserythropoietic anemia and myopathy syndrome, EHBP1L1-related, dog | | MONDO:1012402 | caprine-like generalized hypoplasia syndrome, cattle | caprine-like generalized hypoplasia syndrome, CEP250-related, cattle | | MONDO:1011250 | leber congenital amaurosis, dog | leber congenital amaurosis, RPE65-related, dog | | MONDO:1012427 | muscular dystrophy-dystroglycanopathy (limb-girdle), domestic cat | muscular dystrophy-dystroglycanopathy (limb-girdle), COLQ-related, domestic cat | | MONDO:1012401 | dilute coat color with neurological defects, horse | dilute coat color with neurological defects, MYO5A-related, horse | | MONDO:1010633 | factor VII deficiency, Asiatic elephant | factor VII deficiency, F7-related, Asiatic elephant | | MONDO:1011481 | beta-mannosidosis, cattle | beta-mannosidosis, MANBA-related, cattle | | MONDO:1010785 | incontinentia pigmenti, horse | incontinentia pigmenti, IKBKG-related, horse | | MONDO:1012087 | alpha fucosidosis, dog | alpha fucosidosis, FUCA1-related, dog | | MONDO:1010603 | congenital hypothyroidism, domestic cat | congenital hypothyroidism, TPO-related, domestic cat | | MONDO:1012537 | hypopigmentation and deafness, pig | hypopigmentation and deafness, KIT-related, pig | | MONDO:1010707 | porphyria cutanea tarda, sheep | porphyria cutanea tarda, UROD-related, sheep | | MONDO:1012497 | Lundehund syndrome, dog | Lundehund syndrome, P3H2-related, dog | | MONDO:0006835 | lipoid nephrosis | minimal change disease | | MONDO:1012420 | brachygnathia, cardiomegaly and renal hypoplasia syndrome, sheep | brachygnathia, cardiomegaly and renal hypoplasia syndrome, OBSL1-related, sheep | | MONDO:1010677 | microtia, sheep | microtia, HMX1-related, sheep | | MONDO:1010522 | frontonasal dysplasia, cattle | frontonasal dysplasia, ZIC2-related, cattle | | MONDO:1012517 | exercise induced metabolic myopathy, dog | exercise induced metabolic myopathy, ACADVL-related, dog | | MONDO:1010716 | acute intermittent porphyria, domestic cat | acute intermittent porphyria, HMBS-related, domestic cat | | MONDO:1012055 | cyclic neutropenia, dog | cyclic neutropenia, AP3B1-related, dog | | MONDO:1010864 | alpha-mannosidosis, domestic cat | alpha-mannosidosis, MAN2B1-related, domestic cat | | MONDO:0700039 | bladder exstrophy-epispadias-cloacal extrophy complex | bladder exstrophy-epispadias-cloacal exstrophy complex | | MONDO:1012393 | growth-hormone deficiency dwarfism, dog | growth-hormone deficiency dwarfism, GH1-related, dog | | MONDO:1010666 | Scott Syndrome, dog | Scott Syndrome, ANO6-related, dog | | MONDO:1011155 | Marfan syndrome, pig | Marfan syndrome, FBN1-related, pig | | MONDO:1012285 | ventricular arrhythmias and sudden death, dog | ventricular arrhythmias and sudden death, MICOS13-related, dog | | MONDO:1012196 | ocular squamous cell carcinoma, horse | ocular squamous cell carcinoma, DDB2-related, horse | | MONDO:1012450 | leukoencephalomyelopathy, dog | leukoencephalomyelopathy, NAPEPLD-related, dog | | MONDO:1011539 | hypokalaemic periodic paralysis, domestic cat | hypokalaemic periodic paralysis, WNK4-related, domestic cat | | MONDO:1010783 | ectodermal dysplasia/skin fragility syndrome, dog | ectodermal dysplasia/skin fragility syndrome, PKP1-related, dog | | MONDO:1012305 | hypocatalasia, dog | hypocatalasia, CAT-related, dog | | MONDO:1012247 | rod-cone dysplasia, domestic cat | rod-cone dysplasia, CRX-related, domestic cat | | MONDO:1010714 | multiple acyl-CoA dehydrogenase deficiency, domestic cat | multiple acyl-CoA dehydrogenase deficiency, ETFDH-related, domestic cat | | MONDO:1011251 | leber congenital amaurosis, domestic cat | leber congenital amaurosis, AIPL1-related, domestic cat | | MONDO:1012369 | renal cystadenocarcinoma and nodular dermatofibrosis, dog | renal cystadenocarcinoma and nodular dermatofibrosis, FLCN-related, dog | | MONDO:1010627 | Chediak-Higashi syndrome, American mink | Chediak-Higashi syndrome, American mink, LYST-related, alpaca | | MONDO:1010653 | polycythemia, dog | polycythemia, JAK2-related, dog | | MONDO:1011019 | L-2-hydroxyglutaricacidemia, domestic cat | L-2-hydroxyglutaricacidemia, L2HGDH-related, domestic cat | | MONDO:1010589 | familial goiter, goat | familial goiter, TG-related, goat | | MONDO:1010796 | Darier disease, dog | Darier disease, ATP2A2-related, dog | | MONDO:1012079 | fibrodysplasia ossificans, domestic cat | fibrodysplasia ossificans, ACVR1-related, domestic cat | | MONDO:1012185 | necrotising myelopathy, dog | necrotising myelopathy, IBA57-related, dog | | MONDO:1011053 | polycystic kidney disease, dog | polycystic kidney disease, PKD1-related, dog | | MONDO:1010924 | muscular dystrophy, Duchenne type, domestic cat | muscular dystrophy, Duchenne type, DMD-related, domestic cat | | MONDO:1012116 | congenital hypomyelinogenesis, cattle | congenital hypomyelinogenesis, KIF1C-related, cattle | | MONDO:1012568 | congenital mast cell tumor, cattle | congenital mast cell tumor, PLP2-related, cattle | | MONDO:1012534 | pulmonary surfactant metabolism dysfunction, dog | pulmonary surfactant metabolism dysfunction, LAMP3-related, dog | | MONDO:1010676 | microtia, pig | microtia, HOXA1-related, pig | | MONDO:1010950 | familial adenomatous polyposis, dog | familial adenomatous polyposis, APC-related, dog | | MONDO:1011596 | severe combined immunodeficiency disease, dog | severe combined immunodeficiency disease, PRKDC-related, dog | | MONDO:1010602 | congenital hypothyroidism, dog | congenital hypothyroidism, TPO-related, dog |

</details>

<details> <summary>Synonyms added: 47</summary>

| Term | New Synonym | Predicate | ----|----|----| | split cord malformation type II (MONDO:1060221) | SCM type II | oio:hasExactSynonym | | TSEN2-related neurodevelopmental disorder with or without thrombotic microangiopathy (MONDO:1060216) | TSEN2-related neurodevelopmental disorder with or without thrombotic microangiopathy | oio:hasExactSynonym | | split cord malformation, composite type (MONDO:1060222) | split cord malformation, intermediate type | oio:hasExactSynonym | | split cord malformation type II (MONDO:1060221) | split cord malformation type 2 | oio:hasExactSynonym | | macrothrombocytopenia and granulocyte inclusions with or without nephritis or sensorineural hearing loss (MONDO:0015912) | MHA | oio:hasExactSynonym | | split cord malformation type I (MONDO:1060220) | SCM type 1 | oio:hasExactSynonym | | celiac trunk compression syndrome (MONDO:0017388) | Median Arcuate Ligament Syndrome | oio:hasExactSynonym | | Meier-Gorlin syndrome 9 (MONDO:0980992) | Meier-Gorlin syndrome 9 | oio:hasExactSynonym | | FAS-related autoimmune lymphoproliferative immune disorder (MONDO:1060194) | FAS-related autoimmune lymphoproliferative immune disorder | oio:hasExactSynonym | | Shwachman-Diamond syndrome 2 (MONDO:0044205) | EFL1-related Shwachman-Diamond syndrome | oio:hasExactSynonym | | GRIN-related complex neurodevelopmental disorder (MONDO:1060138) | GRIN-related encephalopathy | oio:hasExactSynonym | | extraoral halitosis due to methanethiol oxidase deficiency (MONDO:0029144) | autosomal recessive extra-oral halitosis | oio:hasExactSynonym | | southern tick-associated rash illness (MONDO:1010205) | STARI | oio:hasExactSynonym | | macrothrombocytopenia and granulocyte inclusions with or without nephritis or sensorineural hearing loss (MONDO:0015912) | FTNS | oio:hasExactSynonym | | GRIN-related complex neurodevelopmental disorder (MONDO:1060138) | GRIN-related neurodevelopmental disorder | oio:hasExactSynonym | | macrothrombocytopenia and granulocyte inclusions with or without nephritis or sensorineural hearing loss (MONDO:0015912) | MYH9 related disorders | oio:hasExactSynonym | | diastematomyelia (MONDO:0009106) | split spinal cord malformation | oio:hasExactSynonym | | split cord malformation, composite type (MONDO:1060222) | split cord malformation type 1.5 | oio:hasExactSynonym | | GRIN-related complex neurodevelopmental disorder (MONDO:1060138) | GRINpathies | oio:hasExactSynonym | | diastematomyelia (MONDO:0009106) | split cord malformation | oio:hasExactSynonym | | Meier-Gorlin syndrome 9 (MONDO:0980992) | GINS3 Meier-Gorlin syndrome | oio:hasExactSynonym | | split cord malformation, composite type (MONDO:1060222) | split cord malformation, mixed type | oio:hasExactSynonym | | split cord malformation type II (MONDO:1060221) | diplomyelia | oio:hasExactSynonym | | arhinia, choanal atresia, and microphthalmia (MONDO:0011323) | Bosma syndrome | oio:hasExactSynonym | | arhinia, choanal atresia, and microphthalmia (MONDO:0011323) | Gifford-Bosma syndrome | oio:hasExactSynonym | | RNU12-related minor spliceopathy disorder (MONDO:1060223) | RNU12-related minor spliceopathy disorder | oio:hasExactSynonym | | chronic myeloid leukemia (MONDO:0011996) | leukimia, chronic myeloid | oio:hasExactSynonym | | diastematomyelia (MONDO:0009106) | SSCM | oio:hasExactSynonym | | split cord malformation type II (MONDO:1060221) | SCM type 2 | oio:hasExactSynonym | | lymphocytic hypophysitis (MONDO:0019835) | primary hypophysitis | oio:hasRelatedSynonym | | diastematomyelia (MONDO:0009106) | SCM type 1 | oio:hasNarrowSynonym | | arhinia, choanal atresia, and microphthalmia (MONDO:0011323) | BAM syndrome | oio:hasExactSynonym | | short-rib thoracic dysplasia 22 without polydactyly (MONDO:0979242) | thoracic dysostosis, isolated | oio:hasExactSynonym | | myofibrillar myopathy 4 (MONDO:0012277) | LDB3-related myofibrillar myopathy | oio:hasExactSynonym | | macrothrombocytopenia and granulocyte inclusions with or without nephritis or sensorineural hearing loss (MONDO:0015912) | MATINS | oio:hasExactSynonym | | macrothrombocytopenia and granulocyte inclusions with or without nephritis or sensorineural hearing loss (MONDO:0015912) | SBS | oio:hasExactSynonym | | Meier-Gorlin syndrome 9 (MONDO:0980992) | MGORS9 | oio:hasExactSynonym | | autosomal dominant nonsyndromic hearing loss 91 (MONDO:0981166) | deafness, autosomal dominant 91 | oio:hasExactSynonym | | multiple mitochondrial dysfunctions syndrome 7 (MONDO:0957382) | GCSH-related glycine encephalopathy | oio:hasExactSynonym | | macrothrombocytopenia and granulocyte inclusions with or without nephritis or sensorineural hearing loss (MONDO:0015912) | Alport syndrome with macrothrombocytopenia | oio:hasExactSynonym | | split cord malformation type I (MONDO:1060220) | SCM type I | oio:hasExactSynonym | | arhinia, choanal atresia, and microphthalmia (MONDO:0011323) | Ruprecht Majewski syndrome | oio:hasExactSynonym | | split cord malformation type I (MONDO:1060220) | split cord malformation type 1 | oio:hasExactSynonym | | diastematomyelia (MONDO:0009106) | split cord malformation type 1 | oio:hasNarrowSynonym | | southern tick-associated rash illness (MONDO:1010205) | Masters disease | oio:hasExactSynonym | | macrothrombocytopenia and granulocyte inclusions with or without nephritis or sensorineural hearing loss (MONDO:0015912) | macrothrombocytopenia progressive deafness | oio:hasExactSynonym | | arhinia, choanal atresia, and microphthalmia (MONDO:0011323) | arhinia, choanal atresia, microphthalmia, and hypogonadotropic hypogonadism | oio:hasExactSynonym |

</details>

<details> <summary>Synonyms removed: 12203</summary>

| Term | Removed Synonym | ----|----| | lacrimal apparatus disorder (MONDO:0001854) | lachrymal system disorders | | hypercholesterolemia, familial, 4 (MONDO:0011374) | FHCB1, formerly |

... too many to display.

</details>

<details> <summary>Mappings added: 1635</summary>

| Subject | Predicate | Object | ----|----|----| | ataxia with isolated vitamin E deficiency, TTPA-related, dog (MONDO:7770574) | oio:hasDbXref | OMIA:002922-9615 | | ventricular tachycardia, non-human animal (MONDO:1013248) | oio:hasDbXref | VeNom:4569 | | Sjogren syndrome, domestic cat (MONDO:7770552) | oio:hasDbXref | OMIA:002910-9685 | | xanthomatous hypophysitis (MONDO:1060217) | oio:hasDbXref | SCTID:1186907003 | | sex chromosome difference of sexual development, Przewalski's horse (MONDO:7770494) | oio:hasDbXref | OMIA:002776-9798 |

... too many to display, refer to https://github.com/monarch-initiative/mondo/releases/download/v2026-04-07/mondo_release_diff_changed_terms.tsv and https://github.com/monarch-initiative/mondo/releases/download/v2026-04-07/mondo_release_diff_new_terms.tsv for details.

</details>

<details> <summary>Mappings removed: 39</summary>

| Subject | Predicate | Object | ----|----|----| | neurodevelopmental disorder with involuntary movements (MONDO:0060491) | oio:hasDbXref | MEDGEN:1830103 | | familial sleep-related hypermotor epilepsy (MONDO:0000030) | oio:hasDbXref | MEDGEN:777188 | | celiac trunk compression syndrome (MONDO:0017388) | oio:hasDbXref | MEDGEN:349361 | | lymphocytic hypophysitis (MONDO:0019835) | oio:hasDbXref | Orphanet:95506 | | cardiac, facial, and digital anomalies with developmental delay (MONDO:0032572) | oio:hasDbXref | MEDGEN:1809140 | | creatine phosphokinase, elevated serum (MONDO:0007402) | oio:hasDbXref | UMLS:C1857533 | | Pitt-Hopkins-like syndrome 2 (MONDO:0013690) | oio:hasDbXref | UMLS:C5681528 | | Muggenthaler-Chowdhury-Chioza syndrome (MONDO:0976127) | oio:hasDbXref | UMLS:C5568767 | | obsolete thoracic dysostosis, isolated (MONDO:0008549) | oio:hasDbXref | MESH:C566063 | | pulmonary alveolar proteinosis with hypogammaglobulinemia (MONDO:0020840) | oio:hasDbXref | UMLS:C5680364 | | celiac trunk compression syndrome (MONDO:0017388) | oio:hasDbXref | UMLS:C1861783 | | Pitt-Hopkins-like syndrome 2 (MONDO:0013690) | oio:hasDbXref | GARD:0022416 | | pulmonary alveolar proteinosis with hypogammaglobulinemia (MONDO:0020840) | oio:hasDbXref | MEDGEN:1810375 | | autosomal recessive nonsyndromic hearing loss 48 (MONDO:0012273) | oio:hasDbXref | UMLS:C3553944 | | pulmonary alveolar proteinosis with hypogammaglobulinemia (MONDO:0020840) | oio:hasDbXref | GARD:0022313 | | obsolete split cord malformation (MONDO:0035542) | oio:hasDbXref | Orphanet:573278 | | obsolete thoracic dysostosis, isolated (MONDO:0008549) | oio:hasDbXref | OMIM:187750 | | creatine phosphokinase, elevated serum (MONDO:0007402) | oio:hasDbXref | MEDGEN:347475 | | cardiac, facial, and digital anomalies with developmental delay (MONDO:0032572) | oio:hasDbXref | UMLS:C5681633 | | cardiac, facial, and digital anomalies with developmental delay (MONDO:0032572) | oio:hasDbXref | GARD:0022370 | | cerebellar ataxia with neuropathy and bilateral vestibular areflexia syndrome (MONDO:0044720) | oio:hasDbXref | GARD:0016958 | | diastematomyelia (MONDO:0009106) | oio:hasDbXref | Orphanet:1671 | | complex cortical dysplasia with other brain malformations 5 (MONDO:0014337) | oio:hasDbXref | GARD:0027070 | | Charcot-Marie-Tooth disease X-linked dominant 1 (MONDO:0010549) | oio:hasDbXref | UMLS:C1844863 | | familial sleep-related hypermotor epilepsy (MONDO:0000030) | oio:hasDbXref | UMLS:C3696898 | | Charcot-Marie-Tooth disease X-linked dominant 1 (MONDO:0010549) | oio:hasDbXref | MEDGEN:337104 | | Muggenthaler-Chowdhury-Chioza syndrome (MONDO:0976127) | oio:hasDbXref | MEDGEN:1800190 | | Muggenthaler-Chowdhury-Chioza syndrome (MONDO:0976127) | oio:hasDbXref | GARD:0022068 | | Pitt-Hopkins-like syndrome 2 (MONDO:0013690) | oio:hasDbXref | MEDGEN:1842499 | | cerebellar ataxia with neuropathy and bilateral vestibular areflexia syndrome (MONDO:0044720) | oio:hasDbXref | MEDGEN:330880 | | megalencephaly (MONDO:0016608) | oio:hasDbXref | Orphanet:2477 | | obsolete autosomal recessive extra-oral halitosis (MONDO:0034186) | oio:hasDbXref | Orphanet:562538 | | obsolete split cord malformation type II (MONDO:0035541) | oio:hasDbXref | Orphanet:573253 | | neurodevelopmental disorder with involuntary movements (MONDO:0060491) | oio:hasDbXref | GARD:0022369 | | cerebellar ataxia with neuropathy and bilateral vestibular areflexia syndrome (MONDO:0044720) | oio:hasDbXref | UMLS:C1842586 | | neurodevelopmental disorder with involuntary movements (MONDO:0060491) | oio:hasDbXref | UMLS:C5680303 | | autosomal recessive nonsyndromic hearing loss 48 (MONDO:0012273) | oio:hasDbXref | GARD:0015863 | | familial sleep-related hypermotor epilepsy (MONDO:0000030) | oio:hasDbXref | GARD:0011918 | | autosomal recessive nonsyndromic hearing loss 48 (MONDO:0012273) | oio:hasDbXref | MEDGEN:766858 |

</details>

<details> <summary>Text definitions added: 1060</summary>

| Term | New Text Definition | ----|----| | retroperitoneal neoplasm, non-human animal (MONDO:1013147) | Retroperitoneal neoplasm that occurs in non-human animals. | | benign muscle neoplasm, non-human animal (MONDO:1013130) | Benign muscle neoplasm that occurs in non-human animals. | | acne, non-human animal (MONDO:1013547) | Acne that occurs in non-human animals. | | cerebellar disorder, non-human animal (MONDO:1013387) | Cerebellar disorder that occurs in non-human animals. |

... too many to display, refer to https://github.com/monarch-initiative/mondo/releases/download/v2026-04-07/mondo_release_diff_changed_terms.tsv and https://github.com/monarch-initiative/mondo/releases/download/v2026-04-07/mondo_release_diff_new_terms.tsv for details.

</details>

<details> <summary>Text definitions changed: 3</summary>

| Term | Old Text Definition | New Text Definition | ----|----|----| | lymphocytic hypophysitis (MONDO:0019835) | Immune-mediated inflammation of the pituitary gland often associated with other autoimmune diseases (e.g., hashimoto disease; graves disease; and addison disease). | An autoimmune condition affecting the pituitary gland, characterized by lymphocytic infiltration, commonly presenting with pituitary hormone deficiencies. | | Shwachman-Diamond syndrome 2 (MONDO:0044205) | Shwachman-Diamond syndrome-2 (SDS2) is characterized by exocrine pancreatic dysfunction, hematopoietic abnormalities, short stature, and metaphyseal dysplasia ({1:Stepensky et al., 2017}).nnFor a discussion of genetic heterogeneity of Shwachman-Diamond syndrome, see SDS1 (OMIM:260400). | Any Shwachman-Diamond syndrome in which the cause of the disease is a variation on the EFL1 gene, characterized by exocrine pancreatic dysfunction, hematopoietic abnormalities, short stature, and metaphyseal dysplasia. | | adenohypophysitis (MONDO:0019838) | An autoimmune disease of the pituitary gland which can present with varying degrees of pituitary hormonal impairment and/or with symptoms related to pituitary enlargement. It predominantly affects young women in pregnancy or the peripartum period. | A rare, acquired pituitary hormone deficiency characterized by an inflammation of anterior pituitary with varying degrees of pituitary hormonal impairment and/or with symptoms related to pituitary enlargement. Clinical presentation is variable and includes headaches, visual disturbances, symptoms of adrenal insufficiency, hyperprolactinemia, hypothyroidism and hypogonadism. It most commonly affects young women during pregnancy or postpartum period. |

</details>

<details> <summary>Text definitions removed: 1</summary>

| Term | Removed Text Definition | ----|----| | common variable immunodeficiency (MONDO:0015517) | Common variable immunodeficiency (CVID) comprises a heterogeneous group of diseases characterized by a significant hypogammaglobulinemia of unknown cause, failure to produce specific antibodies after immunizations and susceptibility to bacterial infections, predominantly caused by encapsulated bacteria. |

</details>

<details> <summary>Nodes obsoleted with replacement: 2</summary>

| Term | Replacement | ----|----| | obsolete thoracic dysostosis, isolated (MONDO:0008549) | short-rib thoracic dysplasia 22 without polydactyly (MONDO:0979242) | | obsolete autosomal recessive extra-oral halitosis (MONDO:0034186) | extraoral halitosis due to methanethiol oxidase deficiency (MONDO:0029144) |

</details>

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