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Immunodeficiency due to a late component of complements deficiency
6 OMIM references -
7 associated genes
No signs/symptoms info
PROTEIN INTERACTIONS: 1
Congenital factor II deficiency
1 OMIM reference -
1 associated gene
No signs/symptoms info
Immunodeficiency due to a late component of complements deficiency
Congenital factor II deficiency

C5
(UniProt - OMIM)
 F2
(UniProt - OMIM)
C6
(UniProt - OMIM)
C7
(UniProt - OMIM)
C8A
(UniProt - OMIM)
C8B
(UniProt - OMIM)
C8G
(UniProt - OMIM)
C9
(UniProt - OMIM)

INTERACTOME
ASSOCIATIONS
(click on a score value to see the evidence)
C6
(0.52)
F2


Citations in the biomedical literature:


Immunodeficiency due to a late component of complements deficiency
C5 C6 C7 C8A C8B C8G
C9
Congenital factor II deficiency
F2



Immunodeficiency due to a late component of complements deficiency
Congenital factor II deficiency

Synonym(s):
- Deficiency of complement of terminal pathway
- Immunodeficiency due to a C5 to C9 component complement deficiency
Synonym(s):
- Dysprothrombinemia
- Hypoprothrombinemia
- Prothrombin deficiency
Classification (Orphanet):
- Rare genetic disease
- Rare immune disease
Classification (Orphanet):
- Rare genetic disease
- Rare hematologic 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:
Class of prevalence: <1 / 1 000 000
Average age onset: variable
Average age of death: any age
Type of inheritance: autosomal recessive
External references:
6 OMIM references -
No MeSH references
External references:
1 OMIM reference -
No MeSH references
No signs/symptoms info available.