ODCs

Click node...

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

COMMON GENES: 1
PROTEIN INTERACTIONS: 1

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

Spinocerebellar ataxia type 6

Alternating hemiplegia of childhood


INTERACTOME ASSOCIATIONS (click on a score value to see the evidence)	CACNA1A	(0.63)	ATP1A2

Citations in the biomedical literature:

Spinocerebellar ataxia type 6		Alternating hemiplegia of childhood
	Synonym(s): - SCA6		Synonym(s): - AHC - Alternating hemiplegia in childhood

	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: - Average age onset: - Average age of death: - Type of inheritance: autosomal dominant		Epidemiological data: Class of prevalence: unknown Average age onset: neonatal/infancy Average age of death: any age Type of inheritance: autosomal dominant

	External references: 1 OMIM reference - No MeSH references		External references: 2 OMIM references - 1 MeSH reference: C536589

No signs/symptoms info available.