Cytoscape Web
Click node...

Congenital factor II deficiency
1 OMIM reference -
1 associated gene
No signs/symptoms info
PROTEIN INTERACTIONS: 1
Congenital factor XI deficiency
1 OMIM reference -
1 associated gene
No signs/symptoms info
Congenital factor II deficiency
Congenital factor XI deficiency

F2
(UniProt - OMIM)
 F11
(UniProt - OMIM)

INTERACTOME
ASSOCIATIONS
(click on a score value to see the evidence)
F2
(0.52)
F11


Citations in the biomedical literature:


Congenital factor II deficiency
F2
Congenital factor XI deficiency
F11



Congenital factor II deficiency
Congenital factor XI deficiency

Synonym(s):
- Dysprothrombinemia
- Hypoprothrombinemia
- Prothrombin deficiency
Synonym(s):
- Hemophilia C
- PTA deficiency
- Plasma thromboplastin antecedent deficiency
- Rosenthal factor deficiency
- Rosenthal syndrome
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:
Class of prevalence: <1 / 1 000 000
Average age onset: variable
Average age of death: any age
Type of inheritance: autosomal recessive
Epidemiological data:
Class of prevalence: 1-9 / 1 000 000
Average age onset: variable
Average age of death: normal
Type of inheritance: autosomal dominant
External references:
1 OMIM reference -
No MeSH references
External references:
1 OMIM reference -
No MeSH references
No signs/symptoms info available.