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Charcot-Marie-Tooth disease type 1B
rareA sensorineural peripheral polyneuropathy affecting approximately 1 in 2,500 individuals, and is the most common inherited disorder of the peripheral nervous system. Autosomal dominant, autosomal recessive, and X-linked forms have been recognized.
- Identifiers
- MONDO:0007307 OMIM:118200Orphanet:101082
- Also known as
- Charcot Marie Tooth disease type 1B · Charcot-Marie-Tooth disease type 1 caused by mutation in MPZ · Charcot-Marie-Tooth disease, demyelinating, type 1B · Charcot-Marie-Tooth disease, type 1B · CMT 1B
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