ODCs

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1 OMIM reference -
2 associated genes
No signs/symptoms info

PROTEIN INTERACTIONS: 1

1 associated gene
No signs/symptoms info

Spinocerebellar ataxia type 26

Mendelian susceptibility to mycobacterial diseases due to complete ISG15 deficiency

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


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

Citations in the biomedical literature:

Spinocerebellar ataxia type 26		Mendelian susceptibility to mycobacterial diseases due to complete ISG15 deficiency
	Synonym(s): - SCA26		Synonym(s): - MSMD due to complete ISG15 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: Class of prevalence: <1 / 1 000 000 Average age onset: childhood Average age of death: normal Type of inheritance: autosomal recessive

	External references: 1 OMIM reference - 1 MeSH reference: C537203		External references: No OMIM references No MeSH references

No signs/symptoms info available.