ODCs

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2 OMIM references -
3 associated genes
No signs/symptoms info

PROTEIN INTERACTIONS: 1

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

Familial infantile bilateral striatal necrosis

Spinocerebellar ataxia type 26


INTERACTOME ASSOCIATIONS (click on a score value to see the evidence)	NUP62	(0.49)	EEF2

Citations in the biomedical literature:

Familial infantile bilateral striatal necrosis		Spinocerebellar ataxia type 26
	Synonym(s): - Familial IBSN - Familial infantile striatonigral degeneration - Familial infantile striatonigral necrosis		Synonym(s): - SCA26

	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: Class of prevalence: <1 / 1 000 000 Average age onset: neonatal/infancy Average age of death: - Type of inheritance: autosomal dominant		Epidemiological data: (no data available)

	External references: 2 OMIM references - No MeSH references		External references: 1 OMIM reference - 1 MeSH reference: C537203

No signs/symptoms info available.