Lennox-Gastaut sindrome
rare but severe childhood-onset epilepsy
Press Enter · cited answer in seconds
0 sources
Lennox-Gastaut sindrome
Summary
Lennox-Gastaut sindrome is a designated intractable/rare disease[1]. It draws 219 Wikipedia views per month (designated_intractable_rare_disease category, ranking #74 of 201).[2]
Key Facts
- Lennox-Gastaut sindrome's instance of is recorded as designated intractable/rare disease[3].
- Lennox-Gastaut sindrome's instance of is recorded as class of disease[4].
- Henri Gastaut is named after Lennox-Gastaut sindrome[5].
- William Gordon Lennox is named after Lennox-Gastaut sindrome[6].
- Lennox-Gastaut sindrome is a type of childhood electroclinical syndrome[7].
- Lennox-Gastaut sindrome is a type of disease[8].
- Lennox-Gastaut sindrome's external data available at URL is recorded as http://www.nanbyou.or.jp/entry/4889[9].
- Lennox-Gastaut sindrome's NCI Thesaurus ID is recorded as C84816[10].
- Lennox-Gastaut sindrome's health specialty is recorded as neurology[11].
- Lennox-Gastaut sindrome's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0050561[12].
- Lennox-Gastaut sindrome's exact match is recorded as http://identifiers.org/doid/DOID:0050561[13].
- Lennox-Gastaut sindrome's on focus list of Wikimedia project is recorded as WikiProject Medicine[14].
Why It Matters
Lennox-Gastaut sindrome draws 219 Wikipedia views per month (designated_intractable_rare_disease category, ranking #74 of 201).[2] It has Wikipedia articles in 19 language editions, a strong signal of global cultural recognition.[15] It is known by 19 alternative names across languages and contexts.[16]