ODCs

Click node...

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

COMMON GENES: 1

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

Juvenile myoclonic epilepsy

Juvenile absence epilepsy

Citations in the biomedical literature:

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

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

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

No signs/symptoms info available.