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All terms in MONDO

Label Id Description
white matter hypoplasia-corpus callosum agenesis-intellectual disability syndrome MONDO_0017918
aphonia-deafness-retinal dystrophy-bifid halluces-intellectual disability syndrome MONDO_0017934
hyperinsulinism due to HNF1A deficiency MONDO_0017935
benign Samaritan congenital myopathy MONDO_0017936
autosomal dominant intermediate Charcot-Marie-Tooth disease with neuropathic pain MONDO_0017937
mixed sclerosing bone dystrophy with extra-skeletal manifestations MONDO_0017930
hereditary inclusion body myopathy type 4 MONDO_0017931
muscular hypertrophy-hepatomegaly-polyhydramnios syndrome MONDO_0017932
hypertrophic cardiomyopathy and renal tubular disease due to mitochondrial DNA mutation MONDO_0017933
obsolete Ritter disease MONDO_0005948
septicemic plague MONDO_0005956
obsolete scrub typhus MONDO_0005955
intellectual developmental disorder with paroxysmal dyskinesia or seizures MONDO_0030900
obsolete sex cord-stromal tumor MONDO_0005958
Hermansky-Pudlak syndrome 11 MONDO_0030903
setariasis MONDO_0005957
mitochondrial complex 1 deficiency, nuclear type 36 MONDO_0030902
scarlet fever MONDO_0005952
obsolete sarcocystosis MONDO_0005951
screw worm infectious disease MONDO_0005954