Nuclearly-encoded mitochondrial complex v (atp synthase) deficiency
| Disease Term | Disease ID | Gene Symbol | References |
|---|---|---|---|
| Encephalocardiomyopathy, Mitochondrial, Neonatal, Due To Atp Synthase Deficiency | C3279699 | TMEM70 | 18953340, 21147908, 27604308, 26550569, 21815885, 24485043, 20937241, 22986587, 22433607 |