localized epidermolysis bullosa simplex
epidermolysis bullosa simplex that is characterized by skin blistering that begins anytime between childhood and adulthood and is usually limited to the hands and feet
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localized epidermolysis bullosa simplex
Summary
localized epidermolysis bullosa simplex is a rare disease[1]. It draws 2 Wikipedia views per month (rare_disease category, ranking #237 of 627).[2]
Key Facts
- localized epidermolysis bullosa simplex's instance of is recorded as rare disease[3].
- localized epidermolysis bullosa simplex's instance of is recorded as class of disease[4].
- localized epidermolysis bullosa simplex is a type of epidermolysis bullosa simplex[5].
- localized epidermolysis bullosa simplex is a type of basal epidermolysis bullosa simplex[6].
- localized epidermolysis bullosa simplex is a type of autosomal dominant disease[7].
- localized epidermolysis bullosa simplex's ICD-9-CM is recorded as 757.39[8].
- localized epidermolysis bullosa simplex's genetic association is recorded as KRT14[9].
- localized epidermolysis bullosa simplex's genetic association is recorded as ITGB4[10].
- localized epidermolysis bullosa simplex's genetic association is recorded as KRT5[11].
- localized epidermolysis bullosa simplex's exact match is recorded as http://identifiers.org/doid/DOID:0080510[12].
- localized epidermolysis bullosa simplex's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0080510[13].
- localized epidermolysis bullosa simplex's on focus list of Wikimedia project is recorded as WikiProject Medicine[14].
Why It Matters
localized epidermolysis bullosa simplex draws 2 Wikipedia views per month (rare_disease category, ranking #237 of 627).[2]