ORPHA:64747
X-linked Charcot-Marie-Tooth disease
Also called CMTX, X-linked hereditary motor and sensory neuropathy
- Body system
- Neurological diseases
- Inheritance pattern
- X-linked dominant, X-linked recessive
- Typical age of onset
- Not documented in Orphadata
- Estimated prevalence
- 1-9 / 100 000 (Europe)
- Rarity class
- 1-9 / 100 000
ORPHA:64747 is classified under "Neurological diseases" in the Orphanet nomenclature.