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

F10
(UniProt - OMIM)
 GGCX
(UniProt - OMIM)

INTERACTOME
ASSOCIATIONS
(click on a score value to see the evidence)
F10
(0.52)
GGCX


Citations in the biomedical literature:


Congenital factor X deficiency
F10
Body skin hyperlaxity due to vitamin K-dependent coagulation factor deficiency
GGCX



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

Synonym(s):
- Congenital Stuart factor deficiency
- Stuart-Prower factor deficiency
Synonym(s):
- PXE-like syndrome
- Pseudoxanthoma elasticum-like syndrome
Classification (Orphanet):
- Rare genetic disease
- Rare hematologic disease
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 -
Classification (ICD10):
- Diseases of the blood and blood-forming organs and certain disorders involving the immune mechanism -
Epidemiological data:
Class of prevalence: 1-9 / 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:
1 OMIM reference -
No MeSH references
No signs/symptoms info available.