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Mendelian susceptibility to mycobacterial diseases due to complete ISG15 deficiency
1 associated gene
No signs/symptoms info
PROTEIN INTERACTIONS: 1
Spinocerebellar ataxia type 26
1 OMIM reference -
2 associated genes
No signs/symptoms info
Mendelian susceptibility to mycobacterial diseases due to complete ISG15 deficiency
Spinocerebellar ataxia type 26

ISG15
(UniProt - OMIM)
 EEF2
(UniProt - OMIM)
SCA26
()

INTERACTOME
ASSOCIATIONS
(click on a score value to see the evidence)
ISG15
(0.63)
EEF2


Citations in the biomedical literature:


Mendelian susceptibility to mycobacterial diseases due to complete ISG15 deficiency
ISG15
Spinocerebellar ataxia type 26
EEF2 SCA26



Mendelian susceptibility to mycobacterial diseases due to complete ISG15 deficiency
Spinocerebellar ataxia type 26

Synonym(s):
- MSMD due to complete ISG15 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:
Class of prevalence: <1 / 1 000 000
Average age onset: childhood
Average age of death: normal
Type of inheritance: autosomal recessive
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.