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All terms in MONDO

Label Id Description
autosomal recessive nonsyndromic hearing loss 9 MONDO_0010986
obsolete Coxsackievirus B3 susceptibility MONDO_0007347
Prader-Willi syndrome due to paternal 15q11q13 deletion MONDO_0020301
Mayer-Rokitansky-Küster-Hauser syndrome type 2 MONDO_0010989
cluster headache, familial MONDO_0007344
aplasia cutis-myopia syndrome MONDO_0010988
aorta coarctation MONDO_0007345
isolated congenital digital clubbing MONDO_0007343
cleidorhizomelic syndrome MONDO_0007341
coloboma, ocular, autosomal dominant MONDO_0007350
obsolete classic Hodgkin lymphoma, lymphocyte-rich type MONDO_0020329
47,XYY syndrome MONDO_0019339
obsolete classic Hodgkin lymphoma, mixed cellularity type MONDO_0020328
classic Hodgkin lymphoma, nodular sclerosis type MONDO_0020327
lymphomatoid papulosis MONDO_0020326
iatrogenic Creutzfeldt-Jakob disease MONDO_0034976
mild hyperphenylalaninemia MONDO_0019335
autosomal recessive hyperinsulinism due to Kir6.2 deficiency MONDO_0019334
diazoxide-resistant diffuse hyperinsulinism MONDO_0015625
diomedi bernardi placidi syndrome MONDO_0022989