congenital cataract-progressive muscular hypotonia-hearing loss-developmental delay syndrome

Findings

No curated finding names congenital cataract-progressive muscular hypotonia-hearing loss-developmental delay syndrome yet. Everything below is reference data from Mondo, HPO and GenCC, not evidence about what affects it.

Definition

Inheritance

Autosomal recessive inheritance

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

• inborn mitochondrial myopathy
• mitochondrial oxidative phosphorylation disorder

Resolves to: congenital cataract-progressive muscular hypotonia-hearing loss-developmental delay syndrome

Also called

congenital cataract-progressive muscular hypotonia-deafness-developmental delay syndromemyopathy, mitochondrial progressive, with congenital cataract and developmental delay