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GENATLAS PHENOTYPE

last update : 03-04-2013

Symbol	CMTDID
Location	1q23.3
Name	Charcot-Marie-Tooth, dominant intermediate D
Corresponding gene	MPZ
Other symbol(s)	DI-CMTD
Main clinical features	progressive weakness and atrophy, initially of the peroneal muscles and later of the distal muscles of the arms and motor median NCVs ranging from 25 to 45 m/s
Genetic determination	autosomal dominant
Function/system disorder	neurology
	neurology
Type	disease

Remark(s)