All terms in MONDO
| Label | Id | Description |
|---|---|---|
| autosomal dominant limb-girdle muscular dystrophy type 1E (DES) | MONDO_0018098 | |
| muscular dystrophy, limb-girdle, autosomal dominant | MONDO_0015151 | |
| qualitative or quantitative defects of desmin | MONDO_0016187 | |
| ciliary dyskinesia, primary, 48, without situs inversus | MONDO_0031054 | |
| Weaver-Williams syndrome | MONDO_0018095 | |
| Waardenburg syndrome | MONDO_0018094 | |
| West syndrome | MONDO_0018097 | |
| infancy electroclinical syndrome | MONDO_0000413 | |
| neonatal/infantile epilepsy syndrome | MONDO_0100022 | |
| Weill-Marchesani syndrome | MONDO_0018096 | |
| autosomal genetic disease | MONDO_0000429 | |
| acromelic dysplasia | MONDO_0019695 | |
| microcephaly-brachydactyly-kyphoscoliosis syndrome | MONDO_0018091 | |
| double outlet left ventricle | MONDO_0018090 | |
| arbovirus fever | MONDO_0018093 | |
| Vogt-Koyanagi-Harada disease | MONDO_0018092 | |
| panuveitis | MONDO_0017255 | |
| amelogenesis imperfecta, IIa 1K | MONDO_0031084 | |
| amelogenesis imperfecta | MONDO_0019507 | |
| spermatogenic failure 77 | MONDO_0031083 |