Charcot-Marie-Tooth disease, demyelinating, IIA 1I

Findings

No curated finding names Charcot-Marie-Tooth disease, demyelinating, IIA 1I 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

Infantile onset · Childhood 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

• Charcot-Marie-Tooth disease
• POLR3B-related disorder

Resolves to: Charcot-Marie-Tooth disease, demyelinating, IIA 1I

Also called

Charcot-Marie-Tooth disease neuropathy, IIA 1ICMT1I