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MIRAGE
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 |
|---|---|---|---|
| 629 | CFB | complement factor B | |
| 718 | C3 | complement C3 | |
| 3075 | CFH | complement factor H | |
| 3078 | CFHR1 | complement factor H related 1 | |
| 3426 | CFI | complement factor I | |
| 4179 | CD46 | CD46 molecule | |
| 7056 | THBD | thrombomodulin | |
| 10878 | CFHR3 | complement factor H related 3 |
Related Glycoprotein
| UniProt ID | Protein Name | Source |
|---|---|---|
| P00751 | Complement factor B | |
| P01024 | Complement C3 | |
| P05156 | Complement factor I | |
| P07204 | Thrombomodulin | |
| P08603 | Complement factor H | |
| P15529 | Membrane cofactor protein | |
| Q02985 | Complement factor H-related protein 3 | |
| Q03591 | Complement factor H-related protein 1 |
| UniProt ID | Protein Name | Source |
|---|---|---|
| A0A0A6YVP8 | Complement component factor h |
