Version: 8.0.0
Date: Tue Jan 28 2025
hypertrophic cardiomyopathy 13
DOID:0110319
SummaryAssociated GenesAssociated AllelesAssociated Models
Disease

hypertrophic cardiomyopathy 13

Definition
A familial hypertrophic cardiomyopathy that has_material_basis_in heterozygous mutation in the TNNC1 gene on chromosome 3p21.
Synonyms
  • cardiomyopathy familial hypertrophic 13
  • CMH13
Cross References
Parent Terms
Child Terms
None
Sources of Associations

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      Associated Models

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