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

SAMHD1
(UniProt - OMIM)
 GGCX
(UniProt - OMIM)
TREX1
(UniProt - OMIM)
 VKORC1
(UniProt - OMIM)

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


Citations in the biomedical literature:


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



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

Synonym(s):
(no synonyms)

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 skin and subcutaneous tissue -
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:
2 OMIM references -
1 MeSH reference: C535924
External references:
2 OMIM references -
No MeSH references
No signs/symptoms info available.