| Label | Id | |
|---|---|---|
| BCYM3 | 7232 | |
| IDMDC | 17232 | |
| drayer syndrome | C567232 | |
| chromosome 15q26-Qter deletion syndrome | C567232 | |
| brachyolmia type 3; BCYM3 | http://purl.obolibrary.org/obo/MONDO_0007232 | |
| autosomal dominant brachyolmia | 7232 | |
| proptosis, robin association, clenched hands, and multiple abnormalities | C537232 | |
| disease, neonatal | D007232 | |
| diseases, neonatal | D007232 | |
| neonatal disease | D007232 | |
| neonatal diseases | D007232 | |
| brachyolmia type 3 | 7232 | |
| robin association, clenched hands, and multiple abnormalities proptosis | C537232 | |
| infant, newborn, diseases | D007232 | |
| recessive intellectual disability-motor dysfunction-multiple joint contractures syndrome | 17232 |