atypical hemolytic-uremic syndrome

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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