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Atypical hemolytic uremic syndrome with I factor anomaly
1 OMIM reference -
1 associated gene
8 connected diseases
No signs/symptoms info
Disease Type of connection
Immunodeficiency with factor I anomaly
Atypical hemolytic uremic syndrome with C3 anomaly
Complement component 3 deficiency
Atypical hemolytic uremic syndrome with H factor anomaly
Dense deposit disease
Familial drusen
Immunodeficiency with factor H anomaly
Immunoglobulin-mediated membranoproliferative glomerulonephritis
Synonym(s):
- Atypical HUS with I factor anomaly
- D-HUS with I factor anomaly
- Hemolytic-uremic syndrome without diarrhea with I factor anomaly
- aHUS with I factor anomaly
Classification (Orphanet):
- Rare genetic disease
- Rare hematologic disease
- Rare renal disease
Classification (ICD10):
- Diseases of the blood and blood-forming organs and certain disorders involving the immune mechanism -
Epidemiological data:
(no data available)
External references:
1 OMIM reference -
No MeSH references
Gene symbol UniProt reference OMIM reference
CFI P05156217030
No signs/symptoms info available.