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1 associated gene
No signs/symptoms info
PROTEIN INTERACTIONS: 1
2 OMIM references -
2 associated genes
No signs/symptoms info
Severe combined immunodeficiency due to DNA-PKcs deficiency
Chilblain lupus

PRKDC SAMHD1
TREX1


INTERACTOME
ASSOCIATIONS

(click on a score value to see the evidence)
PRKDC
(0.52)
TREX1



Citations in the biomedical literature:


Severe combined immunodeficiency due to DNA-PKcs deficiency
PRKDC
Chilblain lupus
SAMHD1 TREX1



Severe combined immunodeficiency due to DNA-PKcs deficiency
Chilblain lupus

Synonym(s):
- SCID due to DNA-PKcs deficiency

Synonym(s):
(no synonyms)

Classification (Orphanet):
- Rare genetic disease
- Rare immune 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:
(no data available)
Epidemiological data:
(no data available)

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

No signs/symptoms info available.