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2 OMIM references -
2 associated genes
No signs/symptoms info
PROTEIN INTERACTIONS: 1
2 OMIM references -
2 associated genes
No signs/symptoms info
Hereditary combined deficiency of vitamin K-dependent clotting factors
Chilblain lupus

GGCX SAMHD1
VKORC1 TREX1


INTERACTOME
ASSOCIATIONS

(click on a score value to see the evidence)
VKORC1
(0.63)
TREX1



Citations in the biomedical literature:


Hereditary combined deficiency of vitamin K-dependent clotting factors
GGCX VKORC1
Chilblain lupus
SAMHD1 TREX1



Hereditary combined deficiency of vitamin K-dependent clotting factors
Chilblain lupus

Synonym(s):
- Hereditary combined deficiency of factors II, VII, IX and X

Synonym(s):
(no synonyms)

Classification (Orphanet):
- Inborn errors of metabolism
- 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 skin and subcutaneous tissue -

Epidemiological data:
Class of prevalence: <1 / 1 000 000
Average age onset: neonatal/infancy
Average age of death: -
Type of inheritance: autosomal recessive
Epidemiological data:
(no data available)

External references:
2 OMIM references -
No MeSH references
External references:
2 OMIM references -
1 MeSH reference: C535924

No signs/symptoms info available.