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References OMIM Gene GeneReviews HGMD HGNC
GENATLAS PHENOTYPE
last update : 19/06/2006
Symbol CMH9
Location 2q24.3
Name cardiomyopathy, familial, hypertrophic, 9
Corresponding gene TTN
Genetic determination autosomal dominant
Function/system disorder cardiovascular
neuromuscular
Type disease
Gene product
Name titin,with an altered affinity to alpha-actitin