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

EEF2
(UniProt - OMIM)
 PRKDC
(UniProt - OMIM)
SCA26

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


Citations in the biomedical literature:


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



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

Synonym(s):
- SCA26
Synonym(s):
- SCID due to DNA-PKcs deficiency
Classification (Orphanet):
- Rare genetic disease
- Rare neurologic disease
Classification (Orphanet):
- Rare genetic disease
- Rare immune disease
Classification (ICD10):
- Diseases of the nervous system -
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:
1 OMIM reference -
1 MeSH reference: C537203
External references:
No OMIM references
No MeSH references
No signs/symptoms info available.