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Mondo Disease Ontology
MONDO
All terms in MONDO
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Label
Id
Description
hypertrichotic osteochondrodysplasia Cantu type
MONDO_0009406
cervical hypertrichosis-peripheral neuropathy syndrome
MONDO_0009405
hypertelorism, microtia, facial clefting syndrome
MONDO_0009404
hypertelorism and tetralogy of fallot
MONDO_0009403
acrofrontofacionasal dysostosis 2
MONDO_0009402
hyperprolinemia type 2
MONDO_0009401
hyperprolinemia
MONDO_0023419
hyperprolinemia type 1
MONDO_0009400
X-linked scapuloperoneal muscular dystrophy
MONDO_0010400
syndromic X-linked intellectual disability 94
MONDO_0010402
X-linked myopathy with postural muscle atrophy
MONDO_0010401
Woodhouse-Sakati syndrome
MONDO_0009419
hypogonadism with low-grade mental deficiency and microcephaly
MONDO_0009418
hypergonadotropic hypogonadism-cataract syndrome
MONDO_0009417
hypoinsulinemic hypoglycemia and body hemihypertrophy
MONDO_0009416
hypoglycemia, leucine-induced
MONDO_0009415
glycogen storage disorder due to hepatic glycogen synthase deficiency
MONDO_0009414
immunodeficiency, common variable, 2
MONDO_0009413
scurvy
MONDO_0009412
autoimmune polyendocrine syndrome type 1
MONDO_0009411