Nuclearly-encoded mitochondrial complex v (atp synthase) deficiency
| Disease Term | Disease ID | Gene Symbol | Classification | References | Source |
|---|---|---|---|---|---|
| Encephalocardiomyopathy, Mitochondrial, Neonatal, Due To Atp Synthase Deficiency | C3279699 | TMEM70 | Unknown Evidence from: GenCC, GWAS, ClinVar (non-pathogenic), CBGDA, or Text Mining associations | 18953340, 20937241, 21147908, 21815885, 22433607, 22986587, 24485043, 26550569, 27604308 | - |