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C3 glomerulonephritis
1 OMIM reference -
2 associated genes
No signs/symptoms info
PROTEIN INTERACTIONS: 1
Immunodeficiency with factor H anomaly
1 OMIM reference -
1 associated gene
No signs/symptoms info
C3 glomerulonephritis
Immunodeficiency with factor H anomaly

CFHR1
(UniProt - OMIM)
 CFH
(UniProt - OMIM)
CFHR5
(UniProt - OMIM)

INTERACTOME
ASSOCIATIONS
(click on a score value to see the evidence)
CFHR1
(0.62)
CFH


Citations in the biomedical literature:


C3 glomerulonephritis
CFHR1 CFHR5
Immunodeficiency with factor H anomaly
CFH



C3 glomerulonephritis
Immunodeficiency with factor H anomaly

Classification (Orphanet):
- Rare genetic disease
- Rare renal disease
Classification (Orphanet):
- Rare genetic disease
- Rare immune disease
Classification (ICD10):
(no data available)
Classification (ICD10):
- Diseases of the blood and blood-forming organs and certain disorders involving the immune mechanism -
Epidemiological data:
(no data available)
Epidemiological data:
(no data available)
External references:
1 OMIM reference -
No MeSH references
External references:
1 OMIM reference -
No MeSH references
No signs/symptoms info available.