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Body skin hyperlaxity due to vitamin K-dependent coagulation factor deficiency
1 OMIM reference -
1 associated gene
10 connected diseases
No signs/symptoms info
Disease Type of connection
Hereditary combined deficiency of vitamin K-dependent clotting factors
Cerebral sinovenous thrombosis
Congenital factor II deficiency
Congenital factor VII deficiency
Congenital factor X deficiency
Hereditary thrombophilia due to congenital protein C deficiency
Mild hemophilia B
Moderately severe hemophilia B
Severe hemophilia B
Symptomatic form of hemophilia B in female carriers
Synonym(s):
- PXE-like syndrome
- Pseudoxanthoma elasticum-like syndrome
Classification (Orphanet):
- Rare genetic disease
- Rare skin disease
Classification (ICD10):
- Diseases of the blood and blood-forming organs and certain disorders involving the immune mechanism -
Epidemiological data:
(no data available)
External references:
1 OMIM reference -
No MeSH references
Gene symbol UniProt reference OMIM reference
GGCX P38435137167
No signs/symptoms info available.