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Mondo Disease Ontology
MONDO
All terms in MONDO
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Label
Id
Description
IgA glomerulonephritis
MONDO_0005342
hypomyelinating leukodystrophy 2
MONDO_0012125
Pelizaeus-Merzbacher-like disease
MONDO_0017226
microcephaly, short stature, and impaired glucose metabolism 2
MONDO_0014785
moyamoya disease 3
MONDO_0012122
Moyamoya disease
MONDO_0016820
congenital disorder of glycosylation type 1E
MONDO_0012123
severe hypotonia-psychomotor developmental delay-strabismus-cardiac septal defect syndrome
MONDO_0014784
transposition of the great arteries, dextro-looped
MONDO_0012128
leukoencephalopathy, arthritis, colitis, and hypogammaglobulinema
MONDO_0012129
CCDC115-CDG
MONDO_0014789
familial avascular necrosis of femoral head
MONDO_0012126
autosomal recessive limb-girdle muscular dystrophy type 2J
MONDO_0012127
autosomal recessive limb-girdle muscular dystrophy type 2W
MONDO_0014788
obsolete preimplantation embryonic lethality 1
MONDO_0014783
pyruvate dehydrogenase phosphatase deficiency
MONDO_0012120
pyruvate dehydrogenase deficiency
MONDO_0019169
otosclerosis 5
MONDO_0012121
otosclerosis
MONDO_0005349
autosomal recessive limb-girdle muscular dystrophy type 2X
MONDO_0014782