Medical Definition of Familial hypertrophic cardiomyopathy

1. Familial occurrence of hypertrophic cardiomyopathy exhibiting an autosomal dominant pattern of inheritance. Familial cardiomyopathy of various kinds occurs with autosomal dominant inheritance. There is also an asymmetrical form affecting the ventricles and the interventricular septum. (05 Mar 2000)



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Lexicographical Neighbors of Familial Hypertrophic Cardiomyopathy

familial glycinuria
familial goiter
familial high density lipoprotein deficiency
familial hyperbetalipoproteinaemia
familial hyperbetalipoproteinaemia and hyperprebetalipoproteinaemia
familial hypercholesteraemic xanthomatosis
familial hypercholesterolaemia
familial hypercholesterolaemia with hyperlipaemia
familial hypercholesterolemia
familial hyperchylomicronaemia
familial hyperchylomicronaemia with hyperprebetalipoproteinaemia
familial hyperlipoproteinaemia
familial hyperprebetalipoproteinaemia
familial hypertriglyceridaemia
familial hypertriglyceridemia
familial hypertrophic cardiomyopathy (current term)
familial hypobetalipoproteinaemia
familial hypophosphatemic rickets
familial intestinal polyposis
familial juvenile nephrophthisis
familial lipodystrophy
familial lipoprotein lipase deficiency
familial lipoprotein lipase inhibitor
familial mediterranean fever
familial mental retardation 1
familial mental retardation protein
familial microcytic anaemia
familial multiple endocrine adenomatosis

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