benign familial infantile epilepsy
infancy electroclinical syndrome that is characterized by convulsions, with onset at age 3 to 12 months
Press Enter · cited answer in seconds
0 sources
Summary
benign familial infantile epilepsy is a rare disease[1]. It draws 109 Wikipedia views per month (rare_disease category, ranking #236 of 627).[2]
Key Facts
- benign familial infantile epilepsy's instance of is recorded as rare disease[3].
- benign familial infantile epilepsy's instance of is recorded as class of disease[4].
- benign familial infantile epilepsy is a type of infancy electroclinical syndrome[5].
- benign familial infantile epilepsy is a type of Benign infantile epilepsy[6].
- benign familial infantile epilepsy's NCI Thesaurus ID is recorded as C183308[7].
- benign familial infantile epilepsy's health specialty is recorded as neurology[8].
- benign familial infantile epilepsy's genetic association is recorded as PRRT2[9].
- benign familial infantile epilepsy's genetic association is recorded as SCN2A[10].
- benign familial infantile epilepsy's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0060169[11].
- benign familial infantile epilepsy's exact match is recorded as http://identifiers.org/doid/DOID:0060169[12].
- benign familial infantile epilepsy's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_306[13].
- benign familial infantile epilepsy's on focus list of Wikimedia project is recorded as WikiProject Medicine[14].
Why It Matters
benign familial infantile epilepsy draws 109 Wikipedia views per month (rare_disease category, ranking #236 of 627).[2] It is known by 12 alternative names across languages and contexts.[15]