All terms in MONDO
| Label | Id | Description |
|---|---|---|
| WAGR syndrome | MONDO_0008681 | |
| partial deletion of the short arm of chromosome 11 | MONDO_0016893 | |
| Wilms tumor 2 | MONDO_0008680 | |
| idiopathic giant cell myocarditis | MONDO_0018008 | |
| idiopathic cardiomyopathy | MONDO_0005110 | |
| mosaic genome-wide paternal uniparental disomy | MONDO_0018007 | |
| uniparental disomy | MONDO_0700086 | |
| non-hypoproteinemic hypertrophic gastropathy | MONDO_0018009 | |
| gastroesophageal disease | MONDO_0015111 | |
| mitochondrial complex 4 deficiency, nuclear type 11 | MONDO_0033645 | |
| acute megakaryoblastic leukemia without down syndrome | MONDO_0018004 | |
| acute megakaryoblastic leukemia | MONDO_0018872 | |
| nongerminomatous germ cell tumor | MONDO_0021656 | |
| limbic encephalitis with DPP6 antibodies | MONDO_0018003 | |
| limbic encephalitis | MONDO_0015588 | |
| microcornea, rod-cone dystrophy, cataract, and posterior staphyloma 1 | MONDO_0033644 | |
| ovarian neoplasm | MONDO_0021068 | |
| adult-onset distal myopathy due to VCP mutation | MONDO_0018006 | |
| inflammatory bowel disease 30 | MONDO_0033643 | |
| vascular ectasia | MONDO_0021658 |