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All terms in MONDO

Label Id Description
ulnar/fibula ray defect-brachydactyly syndrome MONDO_0012063
choanal atresia-hearing loss-cardiac defects-craniofacial dysmorphism syndrome MONDO_0012064
obsolete age-related hearing impairment MONDO_0000089
obsolete Griscelli syndrome MONDO_0000083
pelvic organ prolapse MONDO_0000082
obsolete ovarian dysgenesis MONDO_0000081
obsolete Oto-palato-digital syndrome MONDO_0000080
polymicrogyria MONDO_0000087
obsolete polydactyly, preaxial MONDO_0000086
obsolete pituitary hormone deficiency, combined MONDO_0000085
obsolete pigmented nodular adrenocortical disease MONDO_0000084
toxicity to dolutegravir MONDO_0036025
Joubert syndrome 3 MONDO_0012078
asperger syndrome, susceptibility to, 2 MONDO_0012079
progressive external ophthalmoplegia MONDO_0005181
familial partial lipodystrophy, Kobberling type MONDO_0012072
ribose-5-P isomerase deficiency MONDO_0012073
obsolete autosomal dominant Charcot-Marie-Tooth disease type 2G MONDO_0012070
congenital generalized lipodystrophy type 1 MONDO_0012071
midface hypoplasia, obesity, developmental delay, and neonatal hypotonia MONDO_0012076