" /> Cardiomyopathy, familial hypertrophic, 13 - CISMeF





Preferred Label : Cardiomyopathy, familial hypertrophic, 13;

Symbol : CMH13;

CISMeF acronym : CMH13;

Type : Phenotype, molecular basis known;

Inheritance : Autosomal dominant;

Molecular basis : Caused by mutation in the slow troponin C gene (TNNC1, 191040.0002);

Prefixed ID : #613243;

Details


You can consult :


Nous contacter.
01/11/2024


[Home] [Top]

© Rouen University Hospital. Any partial or total use of this material must mention the source.