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GENATLAS PHENOTYPE

last update : 12-05-2010

Symbol	HMN2C
Location	5q11.2
Name	neuropathy, distal hereditary motor, type IIC
Corresponding gene	HSPB3
Other symbol(s)	HMNIIC, DHMN2C
Main clinical features	characterized by distal muscle weakness, atrophy of the intrinsic foot and hand muscles
Genetic determination	autosomal dominant
Function/system disorder
Type	disease

Remark(s)