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familial hypertrophic cardiomyopathy
Summary
- Definition
- A hypertrophic cardiomyopathy that is characterized by thickening of the heart muscle and has_material_basis_in autosomal dominant inheritance of one or more gene mutations.
- Super Class
- hypertrophic cardiomyopathy
External Links
- Disease Ontology
- DOID:0080326
- Mondo Disease Ontology
- MeSH
- UMLS
- NCI Thesaurus
- ORDO
- OMIM
Related Genes
| Gene ID | Gene Symbol | Description | Source |
|---|---|---|---|
| 17879 | Myh1 | myosin, heavy polypeptide 1, skeletal muscle, adult | |
| 17882 | Myh2 | myosin, heavy polypeptide 2, skeletal muscle, adult | |
| 17883 | Myh3 | myosin, heavy polypeptide 3, skeletal muscle, embryonic | |
| 17884 | Myh4 | myosin, heavy polypeptide 4, skeletal muscle | |
| 17888 | Myh6 | myosin, heavy polypeptide 6, cardiac muscle, alpha | |
| 53419 | Corin | corin, serine peptidase | |
| 116904 | Alpk3 | alpha-kinase 3 | |
| 140781 | Myh7 | myosin, heavy polypeptide 7, cardiac muscle, beta | |
| 225288 | Fhod3 | formin homology 2 domain containing 3 | |
| 544791 | Myh13 | myosin, heavy polypeptide 13, skeletal muscle |
