ODCs

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

COMMON GENES: 1

9 OMIM references -
7 associated genes
No signs/symptoms info

Juvenile absence epilepsy

Juvenile myoclonic epilepsy

Citations in the biomedical literature:

Juvenile absence epilepsy		Juvenile myoclonic epilepsy
	Synonym(s): - JAE		Synonym(s): (no synonyms)

	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: 1-9 / 100 000 Average age onset: childhood Average age of death: - Type of inheritance: autosomal dominant		Epidemiological data: Class of prevalence: unknown Average age onset: adolescence / young Average age of death: normal Type of inheritance: autosomal dominant

	External references: 1 OMIM reference - 1 MeSH reference: C535495		External references: 9 OMIM references - 1 MeSH reference: D020190

No signs/symptoms info available.