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Charcot-Marie-Tooth disease type X

rare

A subtype of Charcot-Marie-Tooth disease with genetic defects on the X chromosome.

Identifiers: MONDO:0018994 Orphanet:64747
Part of: Charcot-Marie-Tooth disease X-linked disease
Also known as: CMTX · COWCK · X-linked hereditary motor and sensory neuropathy

Subtypes

All diseases Rare only

Disease	ID	Subtypes	Genes
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

Rare disease

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