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All terms in MONDO

Label Id Description
intellectual developmental disorder, autosomal recessive 70 MONDO_0032729
combined oxidative phosphorylation deficiency 39 MONDO_0032726
autosomal dominant Opitz G/BBB syndrome MONDO_0007779
Whipple disease MONDO_0005116
spondyloepimetaphyseal dysplasia with joint laxity, type 3 MONDO_0032724
developmental and epileptic encephalopathy, 74 MONDO_0032725
human granulocytic ehrlichiosis MONDO_0005118
anaplasmosis MONDO_0025303
hypertaurinuric cardiomyopathy MONDO_0007777
obsolete hypertelorism MONDO_0007778
immunodeficiency 60 MONDO_0032723
hypersecretion of adrenal androgens, familial MONDO_0007775
Coronaviridae infectious disease MONDO_0005718
cerebellar ataxia with neuropathy and bilateral vestibular areflexia syndrome MONDO_0044720
hypersensitivity pneumonitis, familial MONDO_0007776
myoclonic epilepsy, juvenile, susceptibility to, 1 MONDO_0020752
orthostatic hypotension 2 MONDO_0020751
hyperproglucagonemia MONDO_0007773
hyperreflexia MONDO_0007774
polycystic lipomembranous osteodysplasia with sclerosing leukoencephalopathy 2 MONDO_0020750