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All terms in MONDO

Label Id Description
combined oxidative phosphorylation defect type 27 MONDO_0014728
immunodeficiency 45 MONDO_0014727
Charcot-Marie-Tooth disease axonal type 2X MONDO_0014726
rhizomelic chondrodysplasia punctata type 5 MONDO_0014743
Parkinson disease 22, autosomal dominant MONDO_0014742
late-onset Parkinson disease MONDO_0008199
DeSanto-Shinawi syndrome due to WAC point mutation MONDO_0014741
autosomal dominant nonsyndromic hearing loss 68 MONDO_0014740
familial progressive retinal dystrophy-iris coloboma-congenital cataract syndrome MONDO_0014747
SLC39A8-CDG MONDO_0014746
congenital myasthenic syndrome 19 MONDO_0014745
acute infantile liver failure-cerebellar ataxia-peripheral sensory motor neuropathy syndrome MONDO_0014744
congenital disorder of glycosylation, type ICC MONDO_0026729
Shukla-Vernon syndrome MONDO_0026727
vulva verrucous carcinoma MONDO_0002758
bladder verrucous carcinoma MONDO_0002759
bladder squamous cell carcinoma MONDO_0002760
hypothyroidism, congenital, nongoitrous, 9 MONDO_0026732
plantar verrucous skin carcinoma MONDO_0002765
obsolete vertigo MONDO_0000102