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C3 glomerulonephritis
1 OMIM reference -
2 associated genes
11 connected diseases
No signs/symptoms info
Disease Type of connection
Atypical hemolytic uremic syndrome with anti-factor H antibodies
Dense deposit disease
Atypical hemolytic uremic syndrome with C3 anomaly
Complement component 3 deficiency
Apolipoprotein A-I deficiency
Atypical hemolytic uremic syndrome with H factor anomaly
Familial drusen
Familial renal amyloidosis due to Apolipoprotein AI variant
Immunodeficiency with factor H anomaly
Immunoglobulin-mediated membranoproliferative glomerulonephritis
Primary systemic amyloidosis
Synonym(s):
(no synonyms)
Classification (Orphanet):
- Rare genetic disease
- Rare renal disease
Classification (ICD10):
(no data available)
Epidemiological data:
(no data available)
External references:
1 OMIM reference -
No MeSH references
Gene symbol UniProt reference OMIM reference
CFHR1 Q03591134371
CFHR5 Q9BXR6608593
No signs/symptoms info available.