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atypical hemolytic-uremic syndrome with I factor anomaly
Disease Summary
Associated Targets (1)
Tbio
1
Uniprot Description An atypical form of hemolytic uremic syndrome. It is a complex genetic disease characterized by microangiopathic hemolytic anemia, thrombocytopenia, renal failure and absence of episodes of enterocolitis and diarrhea. In contrast to typical hemolytic uremic syndrome, atypical forms have a poorer prognosis, with higher death rates and frequent progression to end-stage renal disease.
Mondo Term and Equivalent IDs
MONDO:0013041: atypical hemolytic-uremic syndrome with I factor anomaly
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Counts of Target Development Levels for diseases known to be associated with this disease. If the disease has a valid DOID, targets known to be associated with all child diseases are aggregated. Click "Explore Associated Targets" to view more facets and details for the target list.
Description from UniProt.
DataSources which have contributed target associations to this disease, and the identifiers by which the disease is referenced.
OMIM:612923
Orphanet:93580
MONDO:0013041
High level summary of knowledge for a disease, including descriptions and datasource references.