Charcot-Marie-Tooth disease type 5
MONDO:0010877Mondo
Findings
No curated finding names Charcot-Marie-Tooth disease type 5 yet. Everything below is reference data from Mondo, HPO and GenCC, not evidence about what affects it.
Definition
Hereditary motor and sensory neuropathy type 5 is a rare axonal hereditary motor and sensory neuropathy characterized by slowly progressive distal muscle weakness and atrophy with or without sensory loss resulting in difficulty in walking, foot drop and pes cavus, that may be associated with pyramidal signs (extensor plantar responses, mild increase in tone, brisk tendon reflexes), muscle cramps, pain and spasticity.
Definition from the Mondo Disease Ontology (MONDO:0010877), read 2026-09-29. CC BY 4.0.
Where it sits
Other names
3 names
Resolves to: Charcot-Marie-Tooth disease type 5
- Also called
- Charcot-Marie-Tooth disease-pyramidal features syndromehereditary motor and sensory neuropathy type 5HMSN 5