Unverricht-Lundborg syndrome
Human disease
Press Enter · cited answer in seconds
0 sources
Unverricht-Lundborg syndrome
Summary
Unverricht-Lundborg syndrome is a rare disease[1]. It draws 64 Wikipedia views per month (rare_disease category, ranking #228 of 627).[2]
Key Facts
- Unverricht-Lundborg syndrome is credited with the discovery of Herman Bernhard Lundborg[3].
- Unverricht-Lundborg syndrome is credited with the discovery of Heinrich Unverricht[4].
- Unverricht-Lundborg syndrome's instance of is recorded as rare disease[5].
- Unverricht-Lundborg syndrome's instance of is recorded as class of disease[6].
- Unverricht-Lundborg syndrome is a type of progressive myoclonus epilepsy[7].
- Unverricht-Lundborg syndrome's Commons category is recorded as Unverricht-Lundborg disease[8].
- Unverricht-Lundborg syndrome's NCI Thesaurus ID is recorded as C179710[9].
- Unverricht-Lundborg syndrome's health specialty is recorded as neurology[10].
- Unverricht-Lundborg syndrome's genetic association is recorded as CSTB[11].
- Unverricht-Lundborg syndrome's genetic association is recorded as PRICKLE1[12].
- Unverricht-Lundborg syndrome's exact match is recorded as http://purl.obolibrary.org/obo/DOID_3535[13].
- Unverricht-Lundborg syndrome's exact match is recorded as http://identifiers.org/doid/DOID:3535[14].
- Unverricht-Lundborg syndrome's on focus list of Wikimedia project is recorded as WikiProject Medicine[15].
Body
Works and Contributions
Credited discoveries include Herman Bernhard Lundborg[3], a physician[16], 1868–1943[17], of Sweden[18], awarded the Honorary doctor of the Heidelberg University[19], specialised in race theory[20] and Heinrich Unverricht[4], a physician[21], 1853–1912[22], of Germany[23].
Why It Matters
Unverricht-Lundborg syndrome draws 64 Wikipedia views per month (rare_disease category, ranking #228 of 627).[2] It has Wikipedia articles in 10 language editions, a strong signal of global cultural recognition.[24] It is known by 7 alternative names across languages and contexts.[25]