transmissible spongiform encephalopathy
group of brain diseases induced by prion proteins
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transmissible spongiform encephalopathy
Summary
transmissible spongiform encephalopathy is a designated intractable/rare disease[1]. It draws 1,654 Wikipedia views per month (designated_intractable_rare_disease category, ranking #28 of 201).[2]
Key Facts
- transmissible spongiform encephalopathy's instance of is recorded as designated intractable/rare disease[3].
- transmissible spongiform encephalopathy's instance of is recorded as rare disease[4].
- transmissible spongiform encephalopathy's instance of is recorded as class of disease[5].
- transmissible spongiform encephalopathy's subclass of is recorded as encephalopathy[6].
- transmissible spongiform encephalopathy's subclass of is recorded as neurodegenerative disease with dementia[7].
- transmissible spongiform encephalopathy's Commons category is recorded as Transmissible spongiform encephalopathies[8].
- transmissible spongiform encephalopathy's MeSH descriptor ID is recorded as D017096[9].
- transmissible spongiform encephalopathy's ICD-9 ID is recorded as 046[10].
- transmissible spongiform encephalopathy's ICD-10 ID is recorded as A81[11].
- transmissible spongiform encephalopathy's DiseasesDB is recorded as 25165[12].
- transmissible spongiform encephalopathy's Freebase ID is recorded as /m/01j5jz[13].
- transmissible spongiform encephalopathy's KEGG ID is recorded as H00061[14].
- transmissible spongiform encephalopathy's MeSH tree code is recorded as C10.228.228.800[15].
- transmissible spongiform encephalopathy's MeSH tree code is recorded as C10.574.843[16].
- transmissible spongiform encephalopathy's MeSH tree code is recorded as C01.207.800[17].
- transmissible spongiform encephalopathy's eMedicine ID is recorded as 1168941[18].
- transmissible spongiform encephalopathy's NL CR AUT ID is recorded as ph137022[19].
- transmissible spongiform encephalopathy's NL CR AUT ID is recorded as ph137024[20].
- transmissible spongiform encephalopathy's Disease Ontology ID is recorded as DOID:649[21].
- transmissible spongiform encephalopathy's has cause is recorded as prion[22].
- transmissible spongiform encephalopathy's topic's main category is recorded as Category:Transmissible spongiform encephalopathies[23].
- transmissible spongiform encephalopathy's external data available at URL is recorded as http://www.nanbyou.or.jp/entry/5370[24].
- transmissible spongiform encephalopathy's Encyclopædia Britannica Online ID is recorded as science/spongiform-encephalopathy[25].
- transmissible spongiform encephalopathy's topic has template is recorded as Template:Prion diseases[26].
- transmissible spongiform encephalopathy's Orphanet ID is recorded as 56970[27].
Why It Matters
transmissible spongiform encephalopathy draws 1,654 Wikipedia views per month (designated_intractable_rare_disease category, ranking #28 of 201).[2] It has Wikipedia articles in 21 language editions, a strong signal of global cultural recognition.[28] It is known by 60 alternative names across languages and contexts.[29]