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All terms in MONDO

Label Id Description
autosomal recessive spinocerebellar ataxia 16 MONDO_0014339
NK-cell enteropathy MONDO_0016996
IL21-related infantile inflammatory bowel disease MONDO_0014338
obsolete hereditary epidermolysis bullosa associated with ocular features MONDO_0016997
obsolete complex chromosomal rearrangement MONDO_0016998
complex cortical dysplasia with other brain malformations 5 MONDO_0014337
acute necrotizing encephalopathy of childhood MONDO_0016991
obsolete peeling skin syndrome type B MONDO_0016992
generalized peeling skin syndrome type C MONDO_0016993
hyperammonemic encephalopathy due to carbonic anhydrase VA deficiency MONDO_0014332
disorder of gluconeogenesis MONDO_0019225
Moyamoya disease with early-onset achalasia MONDO_0014331
genetic gastro-esophageal disease MONDO_0015617
obsolete eculizumab, poor response to MONDO_0014330
acquired prothrombin deficiency MONDO_0016990
periosteal chondroma MONDO_0002359
glottis cancer MONDO_0002351
hepatic flexure cancer MONDO_0002357
ascending colon cancer MONDO_0002238
short stature with microcephaly and distinctive facies MONDO_0014347