All diseases

OMIM ID
115195
OMIM term:
CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 2; CMH2
Alternative terms:

(∗) Location:
1q32.1  
(†) Associated OMIM genes:
TNNT2  
(‡) Associated MGI genes:

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Choose a gene on the left to see models here.
* quick link - http://q.sanger.ac.uk/rxyj168p