hypertrophic cardiomyopathy 11

Summary
Synonym
  • CMH11
  • cardiomyopathy familial hypertrophic 11
Definition
A familial hypertrophic cardiomyopathy that has_material_basis_in heterozygous mutation in the ACTC1 gene on chromosome 15q14.
Super Class
familial hypertrophic cardiomyopathy
Disease Ontology
DOID:0110317
Mondo Disease Ontology
OMIM
MGI genotype (from TogoID)
Related Genes
Displaying all 2 entries
Gene ID Gene Symbol Description Source
60 ACTB actin beta
70 ACTC1 actin alpha cardiac muscle 1
Displaying all 2 entries
Gene ID Gene Symbol Description Source
11461 Actb actin, beta
11464 Actc1 actin, alpha, cardiac muscle 1
Displaying all 2 entries
Gene ID Gene Symbol Description Source
29275 Actc1 actin, alpha, cardiac muscle 1
81822 Actb actin, beta
The Human Phenotype Ontology
Displaying entries 1 - 10 of 22 in total
HPO ID HPO Term
HP:0001695 Cardiac arrest
HP:0004749 Atrial flutter
HP:0001635 Congestive heart failure
HP:0011712 Right bundle branch block
HP:0003581 Adult onset
HP:0001279 Syncope
HP:0011462 Young adult onset
HP:0001962 Palpitations
HP:0100749 Chest pain
HP:0001663 Ventricular fibrillation
Displaying 1 entry
Gene ID Gene Symbol Description
70 ACTC1 actin alpha cardiac muscle 1

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Acknowledgements

Supported by JST NBDC Grant Number JPMJND2204

Partly supported by NIH Common Fund Grant #1U01GM125267-01


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Last updated: December 9, 2024