Cytoscape Web
Click node...


1 OMIM reference -
1 associated gene
No signs/symptoms info
PROTEIN INTERACTIONS: 1
1 OMIM reference -
3 associated genes
No signs/symptoms info
Immunodeficiency with factor H anomaly
Atypical hemolytic uremic syndrome with anti-factor H antibodies

CFH CFHR1
CFHR3
CFHR5


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
Atypical hemolytic uremic syndrome with anti-factor H antibodies
CFHR1 CFHR3 CFHR5



Immunodeficiency with factor H anomaly
Atypical hemolytic uremic syndrome with anti-factor H antibodies

Synonym(s):
(no synonyms)

Synonym(s):
- Atypical HUS with anti-factor H antibodies
- D-HUS with anti-factor H antibodies
- Hemolytic-uremic syndrome without diarrhea with anti-factor H antibodies
- aHUS with anti-factor H antibodies

Classification (Orphanet):
- Rare genetic disease
- Rare immune disease
Classification (Orphanet):
- Rare genetic disease
- Rare hematologic disease
- Rare renal disease

Classification (ICD10):
- Diseases of the blood and blood-forming organs and certain disorders involving the immune mechanism -
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.