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Atypical hemolytic uremic syndrome with H factor anomaly
2 OMIM references -
1 associated gene
No signs/symptoms info
COMMON GENES: 1
Immunoglobulin-mediated membranoproliferative glomerulonephritis
1 OMIM reference -
2 associated genes
No signs/symptoms info
Atypical hemolytic uremic syndrome with H factor anomaly
Immunoglobulin-mediated membranoproliferative glomerulonephritis

CFH
(UniProt - OMIM)
 CFH
(UniProt - OMIM)
DGKE
(UniProt - OMIM)

COMMON
GENES 		CFH


Citations in the biomedical literature:


Atypical hemolytic uremic syndrome with H factor anomaly
CFH
Immunoglobulin-mediated membranoproliferative glomerulonephritis
DGKE



Atypical hemolytic uremic syndrome with H factor anomaly
Immunoglobulin-mediated membranoproliferative glomerulonephritis

Synonym(s):
- Atypical HUS with H factor anomaly
- D-HUS with H factor anomaly
- Hemolytic-uremic syndrome without diarrhea with H factor anomaly
- aHUS with H factor anomaly
Synonym(s):
- Ig-mediated MPGN
- Ig-mediated membranoproliferative glomerulonephritis
- Immunoglobulin-mediated MPGN
Classification (Orphanet):
- Rare genetic disease
- Rare hematologic disease
- Rare renal disease
Classification (Orphanet):
- Rare genetic disease
- Rare renal disease
Classification (ICD10):
- Diseases of the blood and blood-forming organs and certain disorders involving the immune mechanism -
Classification (ICD10):
(no data available)
Epidemiological data:
(no data available)
Epidemiological data:
(no data available)
External references:
2 OMIM references -
No MeSH references
External references:
1 OMIM reference -
No MeSH references
No signs/symptoms info available.