All diseases

OMIM ID
612098
OMIM term:
CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 11; CMH11
Alternative terms:

(∗) Location:
15q14  
(†) Associated OMIM genes:
ACTC1  
(‡) Associated MGI genes:

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* quick link - http://q.sanger.ac.uk/jjjjg66p