ODCs

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

COMMON GENES: 1

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

Benign familial epilepsy of childhood with rolandic spikes

Bilateral perisylvian polymicrogyria

GRIN2A	(UniProt - OMIM)		GPR56	(UniProt - OMIM)
SRPX2	(UniProt - OMIM)		SRPX2	(UniProt - OMIM)

Citations in the biomedical literature:

Benign familial epilepsy of childhood with rolandic spikes		Bilateral perisylvian polymicrogyria
	Synonym(s): - Autosomal dominant BECRS - Centrotemporal epilepsy		Synonym(s): (no synonyms)

	Classification (Orphanet): - Rare genetic disease - Rare neurologic disease		Classification (Orphanet): - Rare developmental defect during embryogenesis - Rare genetic disease - Rare neurologic disease

	Classification (ICD10): - Diseases of the nervous system -		Classification (ICD10): - Congenital malformations, deformations and chromosomal abnormalities -

	Epidemiological data: Class of prevalence: unknown Average age onset: childhood Average age of death: normal Type of inheritance: autosomal dominant		Epidemiological data: (no data available)

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

No signs/symptoms info available.