DISEASES

Disease-gene associations mined from literature

Human genes for benign familial infantile epilepsy

Benign familial infantile epilepsy [DOID:0060169]

An infancy electroclinical syndrome that is characterized by convulsions, with onset at age 3 to 12 months.

Synonyms:  benign familial infantile epilepsy,  benign hereditary infantile epilepsy,  benign familial infantile epilepsies,  DOID:0060169,  benign familial infantile convulsion ...

Linkouts:  OMIM #1 #2 #3 #4