subject	subject_label
MONDO:0001153	gender dysphoria
MONDO:0006514	recalcitrant atopic dermatitis
MONDO:0007299	Sotos syndrome 1
MONDO:0007607	Birt-Hogg-Dube syndrome
MONDO:0007779	autosomal dominant Opitz G/BBB syndrome
MONDO:0008347	idiopathic and/or familial pulmonary arterial hypertension
MONDO:0008406	autosomal recessive Emery-Dreifuss muscular dystrophy
MONDO:0008807	apnea, central sleep
MONDO:0010204	lysosomal acid lipase deficiency
MONDO:0011380	leukoencephalopathy with vanishing white matter
MONDO:0011499	Okamoto syndrome
MONDO:0013742	familial mesial temporal lobe epilepsy with febrile seizures
MONDO:0014753	autosomal recessive optic atrophy
MONDO:0015088	autosomal dominant pure spastic paraplegia
MONDO:0015089	autosomal recessive complex spastic paraplegia
MONDO:0015090	autosomal recessive pure spastic paraplegia
MONDO:0015130	acquired chronic primary adrenal insufficiency
MONDO:0015133	quantitative and/or qualitative congenital phagocyte defect
MONDO:0015144	brain inflammatory disease
MONDO:0015179	intestinal disease due to vitamin absorption anomaly
MONDO:0015180	intestinal disease due to fat malabsorption
MONDO:0015208	syndromic esophageal malformation
MONDO:0015210	syndromic gastroduodenal malformation
MONDO:0015211	non-syndromic intestinal malformation
MONDO:0015212	syndromic intestinal malformation
MONDO:0015213	non-syndromic visceral malformation
MONDO:0015214	syndromic visceral malformation
MONDO:0015222	syndromic respiratory or mediastinal malformation
MONDO:0015310	syndromic optic nerve hypoplasia
MONDO:0015323	teratogenic Pierre Robin syndrome
MONDO:0015334	branchial arch or oral-acral syndrome
MONDO:0015338	syndromic craniosynostosis
MONDO:0015359	autosomal dominant hereditary demyelinating motor and sensory neuropathy
MONDO:0015361	autosomal recessive hereditary demyelinating motor and sensory neuropathy
MONDO:0015365	autosomal dominant hereditary sensory and autonomic neuropathy
MONDO:0015366	autosomal recessive hereditary sensory and autonomic neuropathy
MONDO:0015385	external auditory canal aplasia/hypoplasia
MONDO:0015398	hemifacial microsomia
MONDO:0015412	median facial cleft
MONDO:0015415	oblique facial cleft
MONDO:0015418	lateral facial cleft
MONDO:0015478	paramedian facial cleft
MONDO:0015503	nose and cavum anomaly
MONDO:0015504	larynx anomaly
MONDO:0015586	benign familial mesial temporal lobe epilepsy
MONDO:0015620	syndromic urogenital tract malformation
MONDO:0015679	autosomal thrombocytopenia with normal platelets
MONDO:0015682	primary peritoneal tumor
MONDO:0015683	primary malignant peritoneal tumor
MONDO:0015777	adult hypothyroidism
MONDO:0015778	syndromic hypothyroidism
MONDO:0015817	aggressive primary cutaneous T-cell lymphoma
MONDO:0015818	aggressive primary cutaneous B-cell lymphoma
MONDO:0015822	acquired neutropenia
MONDO:0015846	syndromic uterovaginal malformation
MONDO:0015852	excess breast volume or number
MONDO:0015853	deficient breast volume or number
MONDO:0015860	anomaly of puberty or/and menstrual cycle
MONDO:0015921	ARX-related epileptic encephalopathy
MONDO:0015930	respiratory malformation
MONDO:0015950	inherited skin tumor
MONDO:0016034	cleft lip with or without cleft palate
MONDO:0016072	anomaly of puberty or/and menstrual cycle of genetic origin
MONDO:0016109	autosomal recessive distal myopathy
MONDO:0016114	bulbospinal muscular atrophy of childhood
MONDO:0016115	bulbospinal muscular atrophy of adulthood
MONDO:0016125	infectious, fungal or parasitic myopathy
MONDO:0016149	qualitative or quantitative defects of merosin
MONDO:0016150	qualitative or quantitative defects of integrin alpha-7
MONDO:0016152	qualitative or quantitative defects of calpain
MONDO:0016154	qualitative or quantitative defects of myotubularin
MONDO:0016157	qualitative or quantitative defects of fukutin
MONDO:0016172	acquired sensory ganglionopathy
MONDO:0016179	acquired amyloid peripheral neuropathy
MONDO:0016182	qualitative or quantitative defects of protein O-mannose beta1, 2N-acetylglucosaminyltransferase
MONDO:0016183	qualitative or quantitative defects of protein glycosyltransferase-like
MONDO:0016196	qualitative or quantitative defects of emerin
MONDO:0016200	qualitative or quantitative defects of glucosamine (UDP-N-acetyl)-2-epimerase/N-acetylmannosamine kinase
MONDO:0016201	qualitative or quantitative defects of myotilin
MONDO:0016221	temporomandibular joint anomaly
MONDO:0016224	autosomal dominant proximal spinal muscular atrophy
MONDO:0016229	hereditary vascular anomaly
MONDO:0016375	acquired peripheral movement disorder
MONDO:0016434	acquired dermis elastic tissue disorder
MONDO:0016494	regional variant of Guillain-Barre syndrome
MONDO:0016495	functional variant of Guillain-Barre syndrome
MONDO:0016536	autosomal recessive lymphoproliferative disease
MONDO:0016565	syndromic genetic obesity
MONDO:0016599	autosomal dominant secondary polycythemia
MONDO:0016647	autosomal recessive Stickler syndrome
MONDO:0016701	oligoastrocytic tumor
MONDO:0016721	pineal tumor of neuroepithelial tissue
MONDO:0016725	pineal parenchymal tumor of intermediate differenciation
MONDO:0016726	neuronal tumor
MONDO:0016738	primary germ cell tumor of central nervous system
MONDO:0016980	ATR-X-related syndrome
MONDO:0017127	inherited soft tissue tumor
MONDO:0017128	inherited digestive tract tumor
MONDO:0017129	inherited cardiac tumor
MONDO:0017131	hereditary cardiac anomaly
MONDO:0017240	acrodysostosis with multiple hormone resistance
MONDO:0017241	AP4-related intellectual disability and spastic paraplegia
MONDO:0017270	autosomal ichthyosis syndrome
MONDO:0017288	DICER1 syndrome
MONDO:0017302	qualitative or quantitative defects of troponin
MONDO:0017336	fatal infantile hypertrophic cardiomyopathy due to mitochondrial complex I deficiency
MONDO:0017422	adactyly of hand
MONDO:0017429	joint formation defects
MONDO:0017447	congenital absence/hypoplasia of thumb
MONDO:0017448	congenital absence/hypoplasia of fingers excluding thumb
MONDO:0017506	congenital absence/hypoplasia of thumb, unilateral
MONDO:0017507	congenital absence/hypoplasia of thumb, bilateral
MONDO:0017508	congenital absence/hypoplasia of fingers excluding thumb, bilateral
MONDO:0017670	autosomal dominant diffuse mutilating palmoplantar keratoderma
MONDO:0017709	disorder of lipid absorption and transport
MONDO:0017710	congenital systemic veins anomaly
MONDO:0017742	disorder of O-xylosylglycan synthesis
MONDO:0017743	disorder of O-N-acetylgalactosaminylglycan synthesis
MONDO:0017744	disorder of O-xylosyl/N-acetylgalactosaminylglycan synthesis
MONDO:0017745	disorder of O-mannosylglycan synthesis
MONDO:0017756	disorder of pterin metabolism
MONDO:0017912	X-linked pure spastic paraplegia
MONDO:0017914	pure or complex autosomal dominant spastic paraplegia
MONDO:0017915	pure or complex autosomal recessive spastic paraplegia
MONDO:0017916	pure or complex X-linked spastic paraplegia
MONDO:0017961	46,XX disorder of gonadal development
MONDO:0017962	46,XX disorder of sex development induced by fetoplacental androgens excess
MONDO:0017963	46,XX disorder of sex development induced by endogenous maternal-derived androgen
MONDO:0017964	46,XX disorder of sex development induced by exogenous maternal-derived androgen
MONDO:0017966	46,XY disorder of gonadal development
MONDO:0017969	46,XY disorder of sex development of endocrine origin
MONDO:0017974	46,XY disorder of sex development induced by maternal-exposure to endocrine disruptors
MONDO:0018144	congenital myasthenic syndromes with glycosylation defect
MONDO:0018185	congenital anomaly of the great veins
MONDO:0018222	X-linked intellectual disability due to GRIA3 anomalies
MONDO:0018239	aggrecan-related bone disorder
MONDO:0018277	congenital muscular dystrophy with cerebellar involvement
MONDO:0018279	congenital muscular dystrophy without intellectual disability
MONDO:0018292	congenital disorder of glycosylation-related bone disorder
MONDO:0018318	disorder of asparagine metabolism
MONDO:0018384	avascular necrosis of genetic origin
MONDO:0018496	ARX-related encephalopathy-brain malformation spectrum
MONDO:0018529	qualitative or quantitative defects of Torsin-1A-interacting protein 1
MONDO:0018532	adenocarcinoma of liver and intrahepatic biliary tract
MONDO:0018550	spastic paraplegia-optic atrophy-neuropathy and spastic paraplegia-optic atrophy-neuropathy-related disorder
MONDO:0018579	disorder of ketone body transport
MONDO:0018731	lethal multiple congenital anomalies/dysmorphic syndrome
MONDO:0018743	immune-mediated acquired neuromuscular junction disease
MONDO:0018771	congenital anomaly of ventricular septum
MONDO:0018782	type 1 interferonopathy
MONDO:0018786	pontine autosomal dominant microangiopathy with leukoencephalopathy
MONDO:0018788	COL4A1 or COL4A2-related cerebral small vessel disease
MONDO:0018795	syndromic constitutional thrombocytopenia
MONDO:0019054	congenital limb malformation
MONDO:0019063	vascular anomaly
MONDO:0019138	bleeding diathesis due to a collagen receptor defect
MONDO:0019224	inborn disorder of gamma-aminobutyric acid metabolism
MONDO:0019227	inborn disorder of glycerol metabolism
MONDO:0019271	acrokeratoderma
MONDO:0019277	epidermal appendage anomaly
MONDO:0019286	sebaceous gland anomaly
MONDO:0019486	myoclonic epilepsy of infancy
MONDO:0019513	esophageal malformation
MONDO:0019520	syndromic lymphedema
MONDO:0019593	46,XX disorder of sex development induced by fetal androgens excess
MONDO:0019597	46,XY disorder of sex development due to isolated 17,20-lyase deficiency
MONDO:0019608	46,XX disorder of sex development induced by maternal-derived androgen
MONDO:0019714	non-syndromic polydactyly, syndactyly and/or hyperphalangy
MONDO:0019816	anomaly of the tricuspid subvalvular apparatus
MONDO:0019822	arterial duct anomaly
MONDO:0019826	abnormal origin or aberrant course of coronary artery
MONDO:0019831	congenital anomaly of the coronary sinus
MONDO:0019837	atrial appendage anomaly
MONDO:0019998	gastroduodenal malformation
MONDO:0019999	intestinal malformation
MONDO:0020018	cranial malformation
MONDO:0020019	digestive tract malformation
MONDO:0020023	respiratory or mediastinal malformation
MONDO:0020039	46,XX disorder of sex development induced by androgens excess
MONDO:0020069	chronic encephalitis
MONDO:0020081	macrophage or histiocytic tumor
MONDO:0020093	autosomal dominant isolated diffuse palmoplantar keratoderma
MONDO:0020096	autosomal recessive isolated diffuse palmoplantar keratoderma
MONDO:0020125	acquired neuromuscular junction disease
MONDO:0020145	developmental defect of the eye
MONDO:0020146	major induction processes eye anomaly
MONDO:0020147	anophthalmia-microphthalmia syndrome
MONDO:0020148	syndromic aniridia
MONDO:0020155	eyelid border anomaly
MONDO:0020156	syndromic ankyloblepharon
MONDO:0020157	syndromic palpebral coloboma
MONDO:0020162	secondary ectropion
MONDO:0020163	canthal anomaly
MONDO:0020164	epicanthal fold
MONDO:0020165	syndromic epicanthus
MONDO:0020167	malposition of external canthus
MONDO:0020176	palpebral sebaceous gland tumor
MONDO:0020177	pigmented palpebral tumor
MONDO:0020180	palpebral piliary tumor
MONDO:0020181	mesenchymatous palpebral tumor
MONDO:0020193	secretory apparatus of the lacrimal system anomaly
MONDO:0020195	excretory apparatus of the lacrimal system anomaly
MONDO:0020196	anomaly of the secretory and excretory apparatus of the lacrimal system
MONDO:0020205	bulbar conjunctival dermoid or conjunctival dermolipoma
MONDO:0020210	syndromic hyperopia
MONDO:0020211	syndromic keratoconus
MONDO:0020215	syndromic corneal dystrophy
MONDO:0020216	secondary dysgenetic glaucoma
MONDO:0020235	lens size anomaly
MONDO:0020237	lens shape anomaly
MONDO:0020240	syndromic retinitis pigmentosa
MONDO:0020284	heart position anomaly
MONDO:0020285	transposition of the great arteries and conotruncal cardiac anomaly
MONDO:0020286	aortic malformation
MONDO:0020287	pulmonary artery or pulmonary branch anomaly
MONDO:0020288	atrioventricular valve anomaly
MONDO:0020293	ascending aorta anomaly
MONDO:0020294	atrial defect and interatrial communication
MONDO:0020339	X-linked complex spastic paraplegia
MONDO:0020343	alpha-crystallinopathy
MONDO:0020346	synaptic congenital myasthenic syndrome
MONDO:0020732	progeria
MONDO:0021927	arthrogryposis epileptic seizures migrational brain disorder
MONDO:0022397	retinal ciliopathy due to mutation in the retinitis pigmentosa-1 gene
MONDO:0022399	retinal ciliopathy due to mutation in the RPGR gene
MONDO:0022400	retinal ciliopathy due to mutation in the RPGRIP gene
MONDO:0022404	retinal ciliopathy due to mutation in Usher gene
MONDO:0022405	retinal ciliopathy due to mutation in nephronophthisis gene
MONDO:0022407	retinal ciliopathy due to mutation in Bardet-Biedl gene
MONDO:0025511	inherited neuroendocrine tumor
MONDO:0034147	neonatal epileptic encephalopathy due to glutaminase deficiency
MONDO:0034661	syndromic biliary atresia
MONDO:0034901	ATP13A2-related parkinsonism
MONDO:0034954	syndromic vitreoretinopathy
MONDO:0035075	secondary early-onset glaucoma of genetic origin
MONDO:0035160	progressive myoclonic epilepsy with neuroserpin inclusion bodies
MONDO:0035689	syndrome of reduced sensitivity to thyroid hormone
MONDO:0036042	KAT6B-related multiple congenital anomalies syndrome
MONDO:0038268	autoimmune neurological channelopathy
MONDO:0044618	CLCN4-related X-linked intellectual disability syndrome
MONDO:0044655	c12orf65-related combined oxidative phosphorylation defect
MONDO:0044747	human anaplasmosis
MONDO:0100189	apolipoprotein A-I deficiency
MONDO:0100343	antenatal Bartter syndrome
MONDO:0800095	syndrome with synostosis or other joint formation defect
MONDO:0800297	neuronal ceroid lipofuscinosis, late infantile
MONDO:0800342	cap myopathy 2
MONDO:0858986	autosomal dominant spastic paraplegia type 80
MONDO:0858987	autosomal recessive spastic paraplegia type 82
MONDO:0858988	autosomal recessive spastic paraplegia type 83
MONDO:0858989	autosomal recessive spastic paraplegia type 84
MONDO:0858990	autosomal recessive spastic paraplegia type 85
MONDO:0858991	autosomal recessive spastic paraplegia type 86
MONDO:0858992	autosomal recessive spastic paraplegia type 87
