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Congenital alpha2 antiplasmin deficiency
1 OMIM reference -
1 associated gene
No signs/symptoms info
PROTEIN INTERACTIONS: 1
Familial hypodysfibrinogenemia
1 OMIM reference -
3 associated genes
No signs/symptoms info
Congenital alpha2 antiplasmin deficiency
Familial hypodysfibrinogenemia

SERPINF2
(UniProt - OMIM)
 FGA
(UniProt - OMIM)
FGB
(UniProt - OMIM)
FGG
(UniProt - OMIM)

INTERACTOME
ASSOCIATIONS
(click on a score value to see the evidence)
SERPINF2
(0.62)
FGA


Citations in the biomedical literature:


Congenital alpha2 antiplasmin deficiency
SERPINF2
Familial hypodysfibrinogenemia
FGA FGB FGG



Congenital alpha2 antiplasmin deficiency
Familial hypodysfibrinogenemia

Classification (Orphanet):
- Rare genetic disease
- Rare hematologic 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:
(no data available)
External references:
1 OMIM reference -
No MeSH references
External references:
1 OMIM reference -
No MeSH references
No signs/symptoms info available.