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HGNC

GENATLAS PHENOTYPE

last update : 6/09/2006

Symbol	FHCM1
Location	10q24
Name	fatal hypertrophic cardiomyopathy 1
Corresponding gene	COX15
Main clinical features	early-onset
Genetic determination
Function/system disorder	cardiovascular
	neuromuscular
Type	disease

Gene product

Name	cytochrome c oxidase assembly protein 15