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Hypertrophic cardiomyopathy 19

MedGen UID:
450078
Concept ID:
CN077603
Disease or Syndrome
Synonym: Familial hypertrophic cardiomyopathy 19
 
Monarch Initiative: MONDO:0013476

Definition

Any hypertrophic cardiomyopathy in which the cause of the disease is a mutation in the CALR3 gene. [from MONDO]

Term Hierarchy

CClinical test,  RResearch test,  OOMIM,  GGeneReviews,  VClinVar  

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