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1 associated gene
No signs/symptoms info
PROTEIN INTERACTIONS: 1
1 OMIM reference -
1 associated gene
No signs/symptoms info
Severe combined immunodeficiency due to DNA-PKcs deficiency
Autosomal recessive Emery-Dreifuss muscular dystrophy

PRKDC LMNA


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
Autosomal recessive Emery-Dreifuss muscular dystrophy
LMNA



Severe combined immunodeficiency due to DNA-PKcs deficiency
Autosomal recessive Emery-Dreifuss muscular dystrophy

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

Synonym(s):
- EDMD3

Classification (Orphanet):
- Rare genetic disease
- Rare immune disease
Classification (Orphanet):
- Rare cardiac disease
- Rare genetic disease
- Rare neurologic disease

Classification (ICD10):
- Diseases of the blood and blood-forming organs and certain disorders involving the immune mechanism -
Classification (ICD10):
- Diseases of the nervous system -

Epidemiological data:
(no data available)
Epidemiological data:
(no data available)

External references:
No OMIM references
No MeSH references
External references:
1 OMIM reference -
1 MeSH reference: D020389

No signs/symptoms info available.