epidermolysis bullosa
human disease
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epidermolysis bullosa
Summary
epidermolysis bullosa is a designated intractable/rare disease[1]. It draws 15,080 Wikipedia views per month (designated_intractable_rare_disease category, ranking #29 of 201).[2]
Key Facts
- epidermolysis bullosa's instance of is recorded as designated intractable/rare disease[3].
- epidermolysis bullosa's instance of is recorded as class of disease[4].
- epidermolysis bullosa is a type of vesiculobullous skin disease[5].
- epidermolysis bullosa's Commons category is recorded as Epidermolysis bullosa[6].
- epidermolysis bullosa's external data available at URL is recorded as http://www.nanbyou.or.jp/entry/5338[7].
- epidermolysis bullosa's described by source is recorded as The Unified Medical Dictionary (Librairie du Liban, 2009)[8].
- epidermolysis bullosa's ICD-9-CM is recorded as 757.39[9].
- epidermolysis bullosa's NCI Thesaurus ID is recorded as C67383[10].
- epidermolysis bullosa's health specialty is recorded as medical genetics[11].
- epidermolysis bullosa's drug or therapy used for treatment is recorded as phenytoin[12].
- epidermolysis bullosa's exact match is recorded as http://purl.obolibrary.org/obo/DOID_2730[13].
- epidermolysis bullosa's exact match is recorded as http://identifiers.org/doid/DOID:2730[14].
- epidermolysis bullosa's on focus list of Wikimedia project is recorded as WikiProject Medicine[15].
- epidermolysis bullosa's P14541 is recorded as 2aMDBz[16].
Why It Matters
epidermolysis bullosa draws 15,080 Wikipedia views per month (designated_intractable_rare_disease category, ranking #29 of 201).[2] It has Wikipedia articles in 23 language editions, a strong signal of global cultural recognition.[17] It is known by 25 alternative names across languages and contexts.[18]