combined oxidative phosphorylation defect type 25

Findings

No curated finding names combined oxidative phosphorylation defect type 25 yet. Everything below is reference data from Mondo, HPO and GenCC, not evidence about what affects it.

Definition

Inheritance

Autosomal recessive inheritance

Onset and course

Congenital onset

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

• combined oxidative phosphorylation deficiency

Resolves to: combined oxidative phosphorylation defect type 25

Also called

combined oxidative phosphorylation deficiency caused by mutation in MARS2combined oxidative phosphorylation deficiency type 25COXPD25MARS2 combined oxidative phosphorylation deficiency