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All terms in MONDO

Label Id Description
coronary heart disease, susceptibility to, 3 MONDO_0010331
cholestasis-pigmentary retinopathy-cleft palate syndrome MONDO_0012997
severe motor and intellectual disabilities-sensorineural deafness-dystonia syndrome MONDO_0010334
faciocardiomelic syndrome MONDO_0012998
corpus callosum agenesis-intellectual disability-coloboma-micrognathia syndrome MONDO_0010333
orofaciodigital syndrome VIII MONDO_0010336
myopia 15, autosomal dominant MONDO_0012995
AGAT deficiency MONDO_0012996
X-linked cone-rod dystrophy 3 MONDO_0010335
Leber congenital amaurosis 13 MONDO_0012990
muscular dystrophy, non-human animal MONDO_0024965
holoprosencephaly 1 MONDO_0009349
intellectual disability, X-linked 46 MONDO_0010326
hypogonadotropic hypogonadism 6 with or without anosmia MONDO_0012988
intellectual disability, X-linked 77 MONDO_0010329
familial lipochrome histiocytosis MONDO_0009347
phagocytic cell dysfunction MONDO_0024627
microcephaly 7, primary, autosomal recessive MONDO_0012989
alpha-thalassemia-myelodysplastic syndrome MONDO_0010328
histidinuria due to a renal tubular defect MONDO_0009346