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 |