Health / Medical Topics |
Familial Hypertrophic Cardiomyopathy
Hypertrophic cardiomyopathy caused by mutations in the genes encoding components of the sarcomere, in the absence of predisposing conditions. (NCI Thesaurus)
YOU MAY ALSO LIKE
A rare, life-threatening disorder usually appearing during the first few months of life. It is caused by abnormalities in the PRF1, UNC13D,…
A condition that runs in certain families in which at least two members have dysplastic nevi (atypical moles) and have a tendency…
A congenital disorder caused by mutations in the IKBKAP gene. It is characterized by damage of the sympathetic and parasympathetic and sensory…
The Familial Cancer Risk Shared Resource provides Cancer Center investigators with clinical genetic expertise, data on familial genetic syndromes, germline mutations and…
Cancer that occurs in families more often than would be expected by chance. These cancers often occur at an early age, and…
An autosomal dominant disorder characterized by a history of multiple relapses and remissions of pemphigus lesions.