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atypical hemolytic-uremic syndrome
Summary
- Definition
- A complement deficiency that is characterized by mechanical hemolytic anemia, thrombocytopenia, and renal dysfunction.
- Super Class
- complement deficiency
External Links
- Disease Ontology
- DOID:0080301
- Mondo Disease Ontology
- MeSH
- ORDO
- GARD
- MGI genotype (from TogoID)
Related Genes
| Gene ID | Gene Symbol | Description | Source |
|---|---|---|---|
| 570 | BAAT | bile acid-CoA:amino acid N-acyltransferase | |
| 2539 | G6PD | glucose-6-phosphate dehydrogenase | |
| 2821 | GPI | glucose-6-phosphate isomerase | |
| 5277 | PIGA | phosphatidylinositol glycan anchor biosynthesis class A | |
| 5648 | MASP1 | MBL associated serine protease 1 | |
| 8526 | DGKE | diacylglycerol kinase epsilon | |
| 9380 | GRHPR | glyoxylate and hydroxypyruvate reductase |
Related Glycoprotein
| UniProt ID | Protein Name | Source |
|---|---|---|
| P06744 | Glucose-6-phosphate isomerase | |
| P11413 | Glucose-6-phosphate 1-dehydrogenase | |
| P37287 | Phosphatidylinositol N-acetylglucosaminyltransferase subunit A | |
| P48740 | Mannan-binding lectin serine protease 1 | |
| Q9UBQ7 | Glyoxylate reductase/hydroxypyruvate reductase |
