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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 |
|---|---|---|---|
| 6783 | SULT1E1 | sulfotransferase family 1E member 1 | |
| 7167 | TPI1 | triosephosphate isomerase 1 | |
| 7941 | PLA2G7 | phospholipase A2 group VII | |
| 8802 | SUCLG1 | succinate-CoA ligase GDP/ADP-forming subunit alpha | |
| 8972 | MGAM | maltase-glucoamylase | |
| 9197 | SLC33A1 | solute carrier family 33 member 1 | |
| 10555 | AGPAT2 | 1-acylglycerol-3-phosphate O-acyltransferase 2 | |
| 23417 | MLYCD | malonyl-CoA decarboxylase | |
| 23583 | SMUG1 | single-strand-selective monofunctional uracil-DNA glycosylase 1 | |
| 55750 | AGK | acylglycerol kinase |
Related Glycoprotein
