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

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

COMMON
GENES 		CFH


Citations in the biomedical literature:


Immunodeficiency with factor H anomaly
CFH
Immunoglobulin-mediated membranoproliferative glomerulonephritis
DGKE



Immunodeficiency with factor H anomaly
Immunoglobulin-mediated membranoproliferative glomerulonephritis

Synonym(s):
(no synonyms)

Synonym(s):
- Ig-mediated MPGN
- Ig-mediated membranoproliferative glomerulonephritis
- Immunoglobulin-mediated MPGN
Classification (Orphanet):
- Rare genetic disease
- Rare immune 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:
1 OMIM reference -
No MeSH references
External references:
1 OMIM reference -
No MeSH references
No signs/symptoms info available.