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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
COMMON GENES: 1
Hereditary combined deficiency of vitamin K-dependent clotting factors
2 OMIM references -
2 associated genes
No signs/symptoms info
Body skin hyperlaxity due to vitamin K-dependent coagulation factor deficiency
Hereditary combined deficiency of vitamin K-dependent clotting factors

GGCX
(UniProt - OMIM)
 GGCX
(UniProt - OMIM)
VKORC1
(UniProt - OMIM)

COMMON
GENES 		GGCX


Citations in the biomedical literature:


Body skin hyperlaxity due to vitamin K-dependent coagulation factor deficiency
GGCX
Hereditary combined deficiency of vitamin K-dependent clotting factors
VKORC1



Body skin hyperlaxity due to vitamin K-dependent coagulation factor deficiency
Hereditary combined deficiency of vitamin K-dependent clotting factors

Synonym(s):
- PXE-like syndrome
- Pseudoxanthoma elasticum-like syndrome
Synonym(s):
- Hereditary combined deficiency of factors II, VII, IX and X
Classification (Orphanet):
- Rare genetic disease
- Rare skin disease
Classification (Orphanet):
- Inborn errors of metabolism
- 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: neonatal/infancy
Average age of death: -
Type of inheritance: autosomal recessive
External references:
1 OMIM reference -
No MeSH references
External references:
2 OMIM references -
No MeSH references
No signs/symptoms info available.