Version: 8.0.0
Date: Tue Jan 28 2025
hypertrophic cardiomyopathy 20
DOID:0110326
SummaryAssociated GenesAssociated AllelesAssociated Models
Disease

hypertrophic cardiomyopathy 20

Definition
A familial hypertrophic cardiomyopathy that has_material_basis_in heterozygous mutation in the NEXN gene on chromosome 1p31.1.
Synonyms
  • cardiomyopathy familial hypertrophic 20
  • CMH20
Cross References
Parent Terms
Child Terms
None
Sources of Associations

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    Associated Alleles

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      Associated Models

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