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Body skin hyperlaxity due to vitamin K-dependent coagulation factor deficiency
1 OMIM reference -
1 associated gene
No signs/symptoms info
PROTEIN INTERACTIONS: 1
Congenital factor II deficiency
1 OMIM reference -
1 associated gene
No signs/symptoms info
Body skin hyperlaxity due to vitamin K-dependent coagulation factor deficiency
Congenital factor II deficiency

GGCX
(UniProt - OMIM)
 F2
(UniProt - OMIM)

INTERACTOME
ASSOCIATIONS
(click on a score value to see the evidence)
GGCX
(0.62)
F2


Citations in the biomedical literature:


Body skin hyperlaxity due to vitamin K-dependent coagulation factor deficiency
GGCX
Congenital factor II deficiency
F2



Body skin hyperlaxity due to vitamin K-dependent coagulation factor deficiency
Congenital factor II deficiency

Synonym(s):
- PXE-like syndrome
- Pseudoxanthoma elasticum-like syndrome
Synonym(s):
- Dysprothrombinemia
- Hypoprothrombinemia
- Prothrombin deficiency
Classification (Orphanet):
- Rare genetic disease
- Rare skin 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:
1 OMIM reference -
No MeSH references
External references:
1 OMIM reference -
No MeSH references
No signs/symptoms info available.