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1 associated gene
No signs/symptoms info
PROTEIN INTERACTIONS: 2
1 OMIM reference -
2 associated genes
No signs/symptoms info
Severe combined immunodeficiency due to DNA-PKcs deficiency
Spinocerebellar ataxia type 26

PRKDC EEF2
SCA26
()


INTERACTOME
ASSOCIATIONS

(click on a score value to see the evidence)
PRKDC
PRKDC
(0.63)
(0.63)
EEF2
SCA26



Citations in the biomedical literature:


Severe combined immunodeficiency due to DNA-PKcs deficiency
PRKDC
Spinocerebellar ataxia type 26
EEF2 SCA26



Severe combined immunodeficiency due to DNA-PKcs deficiency
Spinocerebellar ataxia type 26

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

Synonym(s):
- SCA26

Classification (Orphanet):
- Rare genetic disease
- Rare immune disease
Classification (Orphanet):
- 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: C537203

No signs/symptoms info available.