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Congenital factor II deficiency
1 OMIM reference -
1 associated gene
No signs/symptoms info
PROTEIN INTERACTIONS: 2
Fetal and neonatal alloimmune thrombocytopenia
6 associated genes
No signs/symptoms info
Congenital factor II deficiency
Fetal and neonatal alloimmune thrombocytopenia

F2
(UniProt - OMIM)
 CD109
(UniProt - OMIM)
GP1BA
(UniProt - OMIM)
GP1BB
(UniProt - OMIM)
ITGA2
(UniProt - OMIM)
ITGA2B
(UniProt - OMIM)
ITGB3
(UniProt - OMIM)

INTERACTOME
ASSOCIATIONS
(click on a score value to see the evidence)
F2
F2
(0.84)
(0.75)
GP1BA
ITGA2B


Citations in the biomedical literature:


Congenital factor II deficiency
F2
Fetal and neonatal alloimmune thrombocytopenia
CD109 GP1BA GP1BB ITGA2 ITGA2B ITGB3



Congenital factor II deficiency
Fetal and neonatal alloimmune thrombocytopenia

Synonym(s):
- Dysprothrombinemia
- Hypoprothrombinemia
- Prothrombin deficiency
Synonym(s):
- NAIT
Classification (Orphanet):
- Rare genetic disease
- Rare hematologic disease
Classification (Orphanet):
- Rare hematologic disease
Classification (ICD10):
- Diseases of the blood and blood-forming organs and certain disorders involving the immune mechanism -
Classification (ICD10):
- Certain conditions originating in the perinatal period -
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.