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Severe combined immunodeficiency due to DNA-PKcs deficiency
1 associated gene
No signs/symptoms info
PROTEIN INTERACTIONS: 1
Laminopathy type Decaudain-Vigouroux
1 associated gene
No signs/symptoms info
Severe combined immunodeficiency due to DNA-PKcs deficiency
Laminopathy type Decaudain-Vigouroux

PRKDC
(UniProt - OMIM)
 LMNA
(UniProt - OMIM)

INTERACTOME
ASSOCIATIONS
(click on a score value to see the evidence)
PRKDC
(0.63)
LMNA


Citations in the biomedical literature:


Severe combined immunodeficiency due to DNA-PKcs deficiency
PRKDC
Laminopathy type Decaudain-Vigouroux
LMNA



Severe combined immunodeficiency due to DNA-PKcs deficiency
Laminopathy type Decaudain-Vigouroux

Synonym(s):
- SCID due to DNA-PKcs deficiency
Synonym(s):
- Laminopathy with severe metabolic syndrome and myopathy
Classification (Orphanet):
- Rare genetic disease
- Rare immune disease
Classification (Orphanet):
- Rare endocrine disease
- Rare genetic disease
Classification (ICD10):
- Diseases of the blood and blood-forming organs and certain disorders involving the immune mechanism -
Classification (ICD10):
- Endocrine, nutritional and metabolic diseases -
Epidemiological data:
(no data available)
Epidemiological data:
(no data available)
External references:
No OMIM references
No MeSH references
External references:
No OMIM references
No MeSH references
No signs/symptoms info available.