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Genes / Proteins / Lipids Glycans / Glycoconjugates Glycomes Pathways / Interactions / Diseases / Organisms
hypertrophic cardiomyopathy
Summary
- Synonym
-
- hypertrophic obstructive cardiomyopathy
- Definition
- An intrinsic cardiomyopathy that is characterized by abnormal thickening (hypertrophy) of the heart without any obvious cause.
- Super Class
- intrinsic cardiomyopathy
External Links
- Disease Ontology
- DOID:11984
- Mondo Disease Ontology
- MeSH
- UMLS
- NCI Thesaurus
- ORDO
- MGI genotype (from TogoID)
- WikiPathways (from TogoID)
Related Genes
| Gene ID | Gene Symbol | Description | Source |
|---|---|---|---|
| 23583 | SMUG1 | single-strand-selective monofunctional uracil-DNA glycosylase 1 | |
| 27306 | HPGDS | hematopoietic prostaglandin D synthase | |
| 27349 | MCAT | malonyl-CoA-acyl carrier protein transacylase | |
| 29925 | GMPPB | GDP-mannose pyrophosphorylase B | |
| 54344 | DPM3 | dolichyl-phosphate mannosyltransferase subunit 3, regulatory | |
| 55624 | POMGNT1 | protein O-linked mannose N-acetylglucosaminyltransferase 1 (beta 1,2-) | |
| 55750 | AGK | acylglycerol kinase | |
| 56052 | ALG1 | ALG1 chitobiosyldiphosphodolichol beta-mannosyltransferase | |
| 57104 | PNPLA2 | patatin like phospholipase domain containing 2 | |
| 64419 | MTMR14 | myotubularin related protein 14 |
Related Glycoprotein
| UniProt ID | Protein Name | Source |
|---|---|---|
| O75390 | Citrate synthase, mitochondrial | |
| O75882 | Attractin | |
| O95528 | Solute carrier family 2, facilitated glucose transporter member 10 | |
| O95822 | Malonyl-CoA decarboxylase, mitochondrial | |
| P00338 | L-lactate dehydrogenase A chain | |
| P00558 | Phosphoglycerate kinase 1 | |
| P04040 | Catalase | |
| P04406 | Glyceraldehyde-3-phosphate dehydrogenase | |
| P04798 | Cytochrome P450 1A1 | |
| P05091 | Aldehyde dehydrogenase, mitochondrial |
