Mitochondrial DNA depletion syndrome 12B (cardiomyopathic type), autosomal recessive

An inherited condition caused by mutation(s) in the SLC25A4 gene, encoding ADP/ATP translocase 1. It is characterized by hypertrophic cardiomyopathy.

Also known as: MTDPS12B, mitochondrial DNA depletion syndrome 12, mitochondrial DNA depletion syndrome 12B (cardiomyopathic type) AR, mitochondrial DNA depletion syndrome 12B (cardiomyopathic type), AR, mitochondrial DNA depletion syndrome 12B (cardiomyopathic type), autosomal recessive, MTDPS12, mitochondrial DNA depletion syndrome 12 (cardiomyopathic type), mitochondrial DNA depletion syndrome type 12

13 clinical trials for this condition and its sub-types, 0 tagged with Mitochondrial DNA depletion syndrome 12B (cardiomyopathic type), autosomal recessive itself.