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Atypical hemolytic uremic syndrome with C3 anomaly
1 OMIM reference -
1 associated gene
No signs/symptoms info
PROTEIN INTERACTIONS: 1
Properdin deficiency
1 OMIM reference -
1 associated gene
No signs/symptoms info
Atypical hemolytic uremic syndrome with C3 anomaly
Properdin deficiency

C3
(UniProt - OMIM)
 CFP
(UniProt - OMIM)

INTERACTOME
ASSOCIATIONS
(click on a score value to see the evidence)
C3
(0.85)
CFP


Citations in the biomedical literature:


Atypical hemolytic uremic syndrome with C3 anomaly
C3
Properdin deficiency
CFP



Atypical hemolytic uremic syndrome with C3 anomaly
Properdin deficiency

Synonym(s):
- Atypical HUS with C3 anomaly
- D-HUS with C3 anomaly
- Hemolytic-uremic syndrome without diarrhea with C3 anomaly
- aHUS with C3 anomaly
Synonym(s):
(no synonyms)
Classification (Orphanet):
- Rare genetic disease
- Rare hematologic disease
- Rare renal disease
Classification (Orphanet):
- Rare genetic disease
- Rare immune 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 -
1 MeSH reference: C537241
No signs/symptoms info available.