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Genes / Proteins / Lipids Glycans / Glycoconjugates Glycomes Pathways / Interactions / Diseases / Organisms
dilated cardiomyopathy 1GG
Summary
- Synonym
-
- CMD1GG
- Definition
- A dilated cardiomyopathy that has_material_basis_in mutation in the SDHA gene on chromosome 5p15.33.
- Super Class
- dilated cardiomyopathy monogenic disease
External Links
- Disease Ontology
- DOID:0110435
- Mondo Disease Ontology
- OMIM
Related Genes
| Gene ID | Gene Symbol | Description | Source |
|---|---|---|---|
| 6392 | SDHD | succinate dehydrogenase complex subunit D | |
| 6517 | SLC2A4 | solute carrier family 2 member 4 | |
| 7941 | PLA2G7 | phospholipase A2 group VII | |
| 9200 | HACD1 | 3-hydroxyacyl-CoA dehydratase 1 | |
| 10135 | NAMPT | nicotinamide phosphoribosyltransferase | |
| 22845 | DOLK | dolichol kinase | |
| 29954 | POMT2 | protein O-mannosyltransferase 2 | |
| 79147 | FKRP | fukutin related protein | |
| 81031 | SLC2A10 | solute carrier family 2 member 10 | |
| 148738 | HJV | hemojuvelin BMP co-receptor |
Related Glycoprotein
- The Human Phenotype Ontology
| HPO ID | HPO Term |
|---|---|
| HP:0012764 | Orthopnea |
| HP:0100578 | Lipoatrophy |
| HP:0002098 | Respiratory distress |
| HP:0008314 | Decreased activity of mitochondrial complex II |
| HP:0000007 | Autosomal recessive inheritance |
| HP:0003593 | Infantile onset |
| HP:0012664 | Reduced left ventricular ejection fraction |
