ODCs

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

PROTEIN INTERACTIONS: 1

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

Childhood absence epilepsy

Spinocerebellar ataxia type 14


INTERACTOME ASSOCIATIONS (click on a score value to see the evidence)	GABRA1	(0.83)	PRKCG

Citations in the biomedical literature:

Childhood absence epilepsy		Spinocerebellar ataxia type 14
	Synonym(s): - Pyknolepsy		Synonym(s): - SCA14

	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: <1 / 1 000 000 Average age onset: - Average age of death: - Type of inheritance: autosomal dominant

	External references: 4 OMIM references - No MeSH references		External references: 1 OMIM reference - 1 MeSH reference: C537196

No signs/symptoms info available.