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MIRAGE
paroxysmal nocturnal hemoglobinuria
Summary
- Definition
- An acquired hemolytic anemia that is characterized by abdominal pain, hematuria, esophageal dysmotility and thrombosis, has_material_basis_in defect in the cell membrane glycosyl phosphatidylinositols that protect red blood cells from the innate complement immune system.
- Super Class
- hemoglobinuria
External Links
- Disease Ontology
- DOID:0060284
- Mondo Disease Ontology
- MeSH
- UMLS
- NCI Thesaurus
- ORDO
- GARD
Related Genes
| Gene ID | Gene Symbol | Description | Source |
|---|---|---|---|
| 718 | C3 | complement C3 | |
| 727 | C5 | complement C5 | |
| 3117 | HLA-DQA1 | major histocompatibility complex, class II, DQ alpha 1 | |
| 3119 | HLA-DQB1 | major histocompatibility complex, class II, DQ beta 1 | |
| 5277 | PIGA | phosphatidylinositol glycan anchor biosynthesis class A | |
| 51604 | PIGT | phosphatidylinositol glycan anchor biosynthesis class T |
Related Glycoprotein
- The Human Phenotype Ontology
| HPO ID | HPO Term |
|---|---|
| HP:0000822 | Hypertension |
| HP:0003641 | Hemoglobinuria |
| HP:0001873 | Thrombocytopenia |
| HP:0001907 | Thromboembolism |
| HP:0001442 | Typified by somatic mosaicism |
| HP:0003581 | Adult onset |
| HP:0004818 | Paroxysmal nocturnal hemoglobinuria |
| HP:0002027 | Abdominal pain |
| HP:0002829 | Arthralgia |
| HP:0000006 | Autosomal dominant inheritance |
