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

LMNA PRKDC


INTERACTOME
ASSOCIATIONS

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



Citations in the biomedical literature:


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



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

Synonym(s):
- Laminopathy with severe metabolic syndrome and myopathy

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

Classification (Orphanet):
- Rare endocrine disease
- Rare genetic disease
Classification (Orphanet):
- Rare genetic disease
- Rare immune disease

Classification (ICD10):
- Endocrine, nutritional and metabolic diseases -
Classification (ICD10):
- Diseases of the blood and blood-forming organs and certain disorders involving the immune mechanism -

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.