All diseases

OMIM ID
192600
OMIM term:
CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 1; CMH1
Alternative terms:
CMH
VENTRICULAR HYPERTROPHY, HEREDITARY
ASYMMETRIC SEPTAL HYPERTROPHY; ASH
HYPERTROPHIC SUBAORTIC STENOSIS, IDIOPATHIC
(∗) Location:
14q11.2   20q11.21   3p25.3   4q35.1  
(†) Associated OMIM genes:
CAV3   MYH7   MYLK2   SLC25A4  
(‡) Associated MGI genes:

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* quick link - http://q.sanger.ac.uk/l615sagw