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MIM:615418 - MITOCHONDRIAL DNA DEPLETION SYNDROME 12B (CARDIOMYOPATHIC TYPE), AUTOSOMAL RECESSIVE; MTDPS12B
Xenbase Genes: slc25a4
Human Disease Resource: MIM
| MONDO:0008922 - Sengers syndrome |
| MONDO:0014175 - mitochondrial DNA depletion syndrome 12B (cardiomyopathic type), autosomal recessive |
| DOID:0080335 - mitochondrial DNA depletion syndrome 12b |
