| Label | Id | |
|---|---|---|
| intellectual disability, autosomal dominant 22 | 12869.0 | |
| mitochondrial complex 5 (ATP synthase) deficiency, nuclear type 6 | 32869.0 | |
| heart valve disease | 2869.0 | |
| coronary arteries congenital malformation | 22869.0 |
| Label | Id | |
|---|---|---|
| intellectual disability, autosomal dominant 22 | 12869.0 | |
| mitochondrial complex 5 (ATP synthase) deficiency, nuclear type 6 | 32869.0 | |
| heart valve disease | 2869.0 | |
| coronary arteries congenital malformation | 22869.0 |