ODCs

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

PROTEIN INTERACTIONS: 1

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

Spinocerebellar ataxia type 26

Amyotrophic lateral sclerosis-parkinsonism-dementia complex

EEF2	(UniProt - OMIM)		PARK7	(UniProt - OMIM)
SCA26			TRPM7	(UniProt - OMIM)


INTERACTOME ASSOCIATIONS (click on a score value to see the evidence)	EEF2	(0.52)	TRPM7

Citations in the biomedical literature:

Spinocerebellar ataxia type 26		Amyotrophic lateral sclerosis-parkinsonism-dementia complex
	Synonym(s): - SCA26		Synonym(s): - Amyotrophic lateral sclerosis-parkinsonism-dementia of Guam - Guam disease - Lytico-Bodig disease - PDALS - Parkinsonism-dementia-ALS complex

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

	Classification (ICD10): - Diseases of the nervous system -		Classification (ICD10): - Diseases of the nervous system -

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

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

No signs/symptoms info available.