Charcot-Marie-Tooth disease type 1
MONDO:0019011Mondo
Findings
No curated finding names Charcot-Marie-Tooth disease type 1 yet. Everything below is reference data from Mondo, HPO and GenCC, not evidence about what affects it.
Definition
Charcot-Marie-Tooth disease type 1 (CMT1) is a group of autosomal dominant demyelinating peripheral neuropathies characterized by distal weakness and atrophy, sensory loss, foot deformities, and slow nerve conduction velocity.
Definition from the Mondo Disease Ontology (MONDO:0019011), read 2026-09-29. CC BY 4.0.
Where it sits
- A kind of
Other names
4 names
Resolves to: Charcot-Marie-Tooth disease type 1
- Also called
- autosomal dominant demyelinating Charcot-Marie-Tooth diseaseCharcot-Marie-Tooth neuropathy type 1CMT1hereditary motor and sensory neuropathy type 1