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

Amyotrophic lateral sclerosis-parkinsonism-dementia complex

Spinocerebellar ataxia type 26

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


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

Citations in the biomedical literature:

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

	Classification (Orphanet): - Rare neurologic disease		Classification (Orphanet): - Rare genetic disease - 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 - No MeSH references		External references: 1 OMIM reference - 1 MeSH reference: C537203

No signs/symptoms info available.