ZFIN Human Disease: benign familial infantile seizures 6

OBO ID: DOID:0081119

Term Name:	benign familial infantile seizures 6		Search Ontology:
Synonyms:	Autosomal dominant nocturnal frontal lobe epilepsy Benign Familial Infantile Seizures, 6 nocturnal frontal lobe epilepsy-4
Definition:	A benign familial infantile epilepsy that is characterized by afebrile partial complex or generalized tonic-clonic seizures occurring between 3 and 12 months of age with a good response to medication and no neurologic sequelae and that has_material_basis_in mutation in the CHRNA2 gene on chromosome 8p21. https://pubmed.ncbi.nlm.nih.gov/25847220/
References:	OMIM:610353
Ontology:	Human Disease ( DOID:0081119 )

Relationships

is a type of:	autosomal dominant disease benign familial infantile epilepsy autosomal dominant disease benign familial infantile epilepsy Show first 5 Terms

OTHER benign familial infantile seizures 6 PAGES

Alliance (1)

GENES INVOLVED

Human Gene	Zebrafish Ortholog	OMIM Term	OMIM Phenotype ID
CHRNA2	chrna2a chrna2b	Epilepsy, nocturnal frontal lobe, type 4	610353

ZEBRAFISH MODELS No data available

PHENOTYPE No data available

CITATIONS: None