Published May 30, 2018
| Version v2018-05-29
Software
Open
monarch-initiative/mondo: 2018-05-29 release
Authors/Creators
- 1. Lawrence Berkeley National Laboratory
Description
New classes:
- vascular bone neoplasm
- glioma susceptibility 1
- familial chronic mucocutaneous candidiasis
- papillary urothelial hyperplasia
- tumor grading characteristic
- nail infection
- general tumor grading characteristic
- dermatosis of eyelid
- eccrine sweat gland hamartoma
- skin appendage disease
- urothelial hyperplasia
- spondyloarthropathy, susceptibility to
- familial acne inversa
- reactive thrombocytosis
- schwannomatosis 1
- renal hypodysplasia/aplasia 1
- appendix neuroendocrine neoplasm
- duodenal neuroendocrine neoplasm
- digestive system neuroendocrine neoplasm
- gallbladder neuroendocrine neoplasm
- disorder of anatomical region
- enterochromaffin cell serotonin-producing pancreatic neuroendocrine tumor
- aniridia 1
- Adams-Oliver syndrome 1
- epilepsy, hot water, 1
- bethlem myopathy 1
- otofaciocervical syndrome 1
- myopathy, tubular aggregate, 1
- Dowling-Degos disease 1
- pulmonary hypertension, primary, 1
- glucocorticoid deficiency 1
- Singleton-Merten syndrome 1
- basal ganglia calcification, idiopathic, 1
- Brown-Vialetto-van Laere syndrome 1
- choroidal dystrophy, central areolar, 1
- AAA1
- renal hypodysplasia/aplasia 3
- aortic valve disease 1
- amyloidosis, primary localized cutaneous, 1
- FRTS1
- DUH1
- GFND1
- Zimmermann-Laband syndrome 1
- MVP1
- progressive external ophthalmoplegia with mitochondrial dna deletions, autosomal dominant 1
- linear skin defects with multiple congenital anomalies 1
- lymphoproliferative syndrome, X-linked, 1
- D-2-hydroxyglutaric aciduria 1
- myopathy, lactic acidosis, and sideroblastic anemia 1
- epilepsy, familial focal, with variable foci 1
- megalencephalic leukoencephalopathy with subcortical cysts 1
- radioulnar synostosis with amegakaryocytic thrombocytopenia 1
- ataxia-telangiectasia-like disorder 1
- frontometaphyseal dysplasia 1
- AAT1
- trichohepatoenteric syndrome 1
- Jervell and Lange-Nielsen syndrome 1
- brittle cornea syndrome 1
- cerebellar ataxia, mental retardation, and dysequilibrium syndrome 1
- Miyoshi muscular dystrophy 1
- Heimler syndrome 1
- pancreatic agenesis 1
- hypertrophic osteoarthropathy, primary, autosomal recessive, 1
- MCOPCB1
- peeling skin syndrome 1
- hyperparathyroidism 4
- herpes simplex encephalitis, susceptibility to, 1
- sick sinus syndrome 1
- ectodermal dysplasia-syndactyly syndrome 1
- cerebroretinal microangiopathy with calcifications and cysts 1
- hypotonia, infantile, with psychomotor retardation and characteristic facies 1
- febrile seizures, familial, 11
- OPA8
- infantile liver failure syndrome 1
- macular dystrophy, vitelliform, 3
- PDA1
- squamous cell intraepithelial neoplasia
- intraepithelial neoplasia
- liver and intrahepatic bile duct neoplasm
- epithelial neoplasm of rectum
- epithelial tumor of colon
- mesenchymal hamartoma
- Astrakhan spotted fever
- Boutonneuse fever
- tumor grade 3 or 4, general grading system
- tumor grade 2 or 3, general grading system
- tumor grade 1, general grading system
- tumor grade X, general grading system
- tumor grade 3, general grading system
- tumor grade 2, general grading system
- tumor grade 1 or 2, general grading system
- tumor grade 4, general grading system
Files
monarch-initiative/mondo-v2018-05-29.zip
Files
(11.9 MB)
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Additional details
Related works
- Is supplement to
- https://github.com/monarch-initiative/mondo/tree/v2018-05-29 (URL)