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Familial Hypertrophic Cardiomyopathy

Go to external page http://purl.obolibrary.org/obo/NCIT_C84773

Hypertrophic cardiomyopathy caused by mutations in the genes encoding components of the sarcomere, in the absence of predisposing conditions. [ ]

Term info

Label

Familial Hypertrophic Cardiomyopathy

Synonyms
  • Familial Hypertrophic Cardiomyopathy
  • Hypertrophic Familial Cardiomyopathy
Preferred Name

Familial Hypertrophic Cardiomyopathy

Semantic Type

Disease or Syndrome

UMLS CUI

C0949658

code

C84773