atypical hemolytic-uremic syndrome
Information
- Disease name
- atypical hemolytic-uremic syndrome
- Disease ID
- DOID:0080301
- Description
- "A complement deficiency that is characterized by mechanical hemolytic anemia, thrombocytopenia, and renal dysfunction." [url:https\://ghr.nlm.nih.gov/condition/atypical-hemolytic-uremic-syndrome#sourcesforpage, url:https\://rarediseases.info.nih.gov/diseases/8702/index#ref_2575, url:https\://www.ncbi.nlm.nih.gov/pubmed/29226095]
Disease area statistics
[No Data.]
Chromosome band
[No Data.]
Annotation
Genes | Mutation | Description | Source | Links |
---|
NCT ID | Status | Phase | Summary | Start date | Completion date |
---|---|---|---|---|---|
NCT01193348 | Completed | Phase 2 | An Open-Label, Multi-Center Clinical Trial of Eculizumab in Pediatric Patients With Atypical Hemolytic-Uremic Syndrome | September 2010 | April 2014 |
NCT01194973 | Completed | Phase 2 | An Open-label, Multi-center Clinical Trial of Eculizumab in Adult Patients With Atypical Hemolytic-uremic Syndrome | July 2010 | February 2014 |
NCT01522183 | Recruiting | Atypical Hemolytic-Uremic Syndrome (aHUS) Registry | April 30, 2012 | December 31, 2025 |
- Disase is a (Disease Ontology)
- DOID:626
- Cross Reference ID (Disease Ontology)
- GARD:8702
- Cross Reference ID (Disease Ontology)
- MESH:D065766
- Cross Reference ID (Disease Ontology)
- ORDO:2134
- OrphaNumber from OrphaNet (Orphanet)
- 2134