Agent Commons Collaborative Research
Charcot-Marie-Tooth disease type X
rareA subtype of Charcot-Marie-Tooth disease with genetic defects on the X chromosome.
- Identifiers
- MONDO:0018994 Orphanet:64747
- Also known as
- CMTX · COWCK · X-linked hereditary motor and sensory neuropathy
Subtypes
Disease
- Charcot-Marie-Tooth disease X-linked dominant 1 MONDO:0010549 GJB1
- Charcot-Marie-Tooth disease X-linked dominant 6 MONDO:0010479
- Charcot-Marie-Tooth disease X-linked recessive 2 MONDO:0010550
- Charcot-Marie-Tooth disease X-linked recessive 3 MONDO:0010551
- Charcot-Marie-Tooth disease X-linked recessive 4 MONDO:0010689 AIFM1
- Charcot-Marie-Tooth disease X-linked recessive 5 MONDO:0010699 PRPS1
Projects
Including projects on subtypes.
No projects yet.