Cytoscape Web
Click node...

Immunodeficiency with factor H anomaly
1 OMIM reference -
1 associated gene
No signs/symptoms info
COMMON GENES: 1
PROTEIN INTERACTIONS: 1
Dense deposit disease
1 OMIM reference -
2 associated genes
No signs/symptoms info
Immunodeficiency with factor H anomaly
Dense deposit disease

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

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


Citations in the biomedical literature:


Immunodeficiency with factor H anomaly
CFH
Dense deposit disease
CFHR1



Immunodeficiency with factor H anomaly
Dense deposit disease

Synonym(s):
(no synonyms)

Synonym(s):
- Membranoproliferative glomerulonephritis type 2
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:
Class of prevalence: 1-9 / 1 000 000
Average age onset: childhood
Average age of death: -
Type of inheritance: autosomal recessive
External references:
1 OMIM reference -
No MeSH references
External references:
1 OMIM reference -
1 MeSH reference: D015432
No signs/symptoms info available.