| Disease Information | ||||||
|---|---|---|---|---|---|---|
| Disease Name | Gene Name | Type | UMLS | Association Type | Score | Source |
| Encephalocardiomyopathy, Mitochondrial, Neonatal, Due To Atp Synthase Deficiency | TMEM70 | disease | C3279699 | Biomarker | 0.7 | disgenet |
| Encephalocardiomyopathy, Mitochondrial, Neonatal, Due To Atp Synthase Deficiency | TMEM70 | disease | C3279699 | GeneticVariation | 0.7 | disgenet |
| Encephalocardiomyopathy, Mitochondrial, Neonatal, Due To Atp Synthase Deficiency | TMEM70 | disease | C3279699 | GermlineCausalMutation | 0.7 | disgenet |
| Encephalocardiomyopathy, Mitochondrial, Neonatal, Due To Atp Synthase Deficiency | TMEM70 | disease | C3279699 | CausalMutation | 0.7 | disgenet |
| click here to return to the previous page | ||||||