ODCs

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

PROTEIN INTERACTIONS: 1

1 OMIM reference -
1 associated gene
No signs/symptoms info

Spinocerebellar ataxia type 26

Autosomal dominant spastic paraplegia type 13

EEF2	(UniProt - OMIM)		HSPD1	(UniProt - OMIM)
SCA26


INTERACTOME ASSOCIATIONS (click on a score value to see the evidence)	EEF2	(0.56)	HSPD1

Citations in the biomedical literature:

Spinocerebellar ataxia type 26		Autosomal dominant spastic paraplegia type 13
	Synonym(s): - SCA26		Synonym(s): - SPG13

	Classification (Orphanet): - Rare genetic disease - 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: Class of prevalence: <1 / 1 000 000 Average age onset: - Average age of death: - Type of inheritance: autosomal dominant

	External references: 1 OMIM reference - 1 MeSH reference: C537203		External references: 1 OMIM reference - 1 MeSH reference: C537485

No signs/symptoms info available.