mitochondrial DNA depletion syndrome 12A (cardiomyopathic type), autosomal dominant

Findings

No curated finding names mitochondrial DNA depletion syndrome 12A (cardiomyopathic type), autosomal dominant yet. Everything below is reference data from Mondo, HPO and GenCC, not evidence about what affects it.

Definition

Inheritance

Autosomal dominant inheritance

Onset and course

Death in infancy · Congenital onset · Neonatal death

HPO, annotations 2026-09-02

What the disease is reported to present with, and how often among people who have it — never how often a feature means the disease. HPO, annotations 2026-09-02.

Germline variants in the gene encoding each protein, as classified by GenCC submitters, each in their own words. Limited, disputed and refuted submissions are listed too.

Where it sits

A kind of

• mitochondrial DNA depletion syndrome

Resolves to: mitochondrial DNA depletion syndrome 12A (cardiomyopathic type), autosomal dominant

Also called

mitochondrial DNA depletion syndrome 12A (cardiomyopathic type) ADmitochondrial DNA depletion syndrome 12a (cardiomyopathic type), autosomal dominant; MTDPS12AMTDPS12A