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Congenital factor II deficiency
1 OMIM reference -
1 associated gene
No signs/symptoms info
PROTEIN INTERACTIONS: 1
Familial renal amyloidosis due to fibrinogen A alpha-chain variant
1 associated gene
No signs/symptoms info
Congenital factor II deficiency
Familial renal amyloidosis due to fibrinogen A alpha-chain variant

F2
(UniProt - OMIM)
 FGA
(UniProt - OMIM)

INTERACTOME
ASSOCIATIONS
(click on a score value to see the evidence)
F2
(0.89)
FGA


Citations in the biomedical literature:


Congenital factor II deficiency
F2
Familial renal amyloidosis due to fibrinogen A alpha-chain variant
FGA



Congenital factor II deficiency
Familial renal amyloidosis due to fibrinogen A alpha-chain variant

Synonym(s):
- Dysprothrombinemia
- Hypoprothrombinemia
- Prothrombin deficiency
Synonym(s):
- Familial amyloid nephropathy due to fibrinogen A alpha-chain variant
- Fibrinogen A alpha-chain amyloidosis
- Hereditary amyloid nephropathy due to fibrinogen A alpha-chain variant
- Hereditary renal amyloidosis due to fibrinogen A alpha-chain variant
Classification (Orphanet):
- Rare genetic disease
- Rare hematologic 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):
- Endocrine, nutritional and metabolic diseases -
Epidemiological data:
Class of prevalence: <1 / 1 000 000
Average age onset: variable
Average age of death: any age
Type of inheritance: autosomal recessive
Epidemiological data:
(no data available)
External references:
1 OMIM reference -
No MeSH references
External references:
No OMIM references
No MeSH references
No signs/symptoms info available.