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Genes / Proteins / Lipids Glycans / Glycoconjugates Glycomes Pathways / Interactions / Diseases / Organisms
myoglobinuria
Summary
- Definition
- A myopathy that is characterized by an increased urinary excretion of myoglobin.
- Super Class
- myopathy
External Links
- Disease Ontology
- DOID:0080108
- Mondo Disease Ontology
- MeSH
- OMIM
Related Genes
| Gene ID | Gene Symbol | Description | Source |
|---|---|---|---|
| 1376 | CPT2 | carnitine palmitoyltransferase 2 | |
| 3030 | HADHA | hydroxyacyl-CoA dehydrogenase trifunctional multienzyme complex subunit alpha | |
| 3032 | HADHB | hydroxyacyl-CoA dehydrogenase trifunctional multienzyme complex subunit beta | |
| 3033 | HADH | hydroxyacyl-CoA dehydrogenase | |
| 3939 | LDHA | lactate dehydrogenase A | |
| 5224 | PGAM2 | phosphoglycerate mutase 2 | |
| 5230 | PGK1 | phosphoglycerate kinase 1 | |
| 5837 | PYGM | glycogen phosphorylase, muscle associated | |
| 9663 | LPIN2 | lipin 2 | |
| 23175 | LPIN1 | lipin 1 |
Related Glycoprotein
- The Human Phenotype Ontology
| HPO ID | HPO Term |
|---|---|
| HP:0100614 | Myositis |
| HP:0003558 | Viral infection-induced rhabdomyolysis |
| HP:0002153 | Hyperkalemia |
| HP:0010969 | Abnormality of glycolipid metabolism |
| HP:0001315 | Reduced tendon reflexes |
| HP:0005521 | Disseminated intravascular coagulation |
| HP:0002905 | Hyperphosphatemia |
| HP:0002913 | Myoglobinuria |
| HP:0008942 | Acute rhabdomyolysis |
| HP:0001265 | Hyporeflexia |
