Genetically-determined epidermolysis bullosa (Q55769): Difference between revisions

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Epidermólise bolhosa (EB) é o nome dado a um grupo heterogêneo de afecções bolhosas que, na maioria dos casos, são decorrentes de defeitos geneticamente determinados em proteínas estruturais da epiderme e junção dermo-epidérmica. As formas genéticas devem ser distinguidas da doença imunobolhosa, epidermólise bolhosa acquisita (qv).
description / endescription / en
 
Epidermolysis bullosa (EB) is the name given to a heterogeneous group of blistering disorders which in the majority of cases are due to genetically-determined defects in structural proteins of the epidermis and dermo-epidermal junction. The genetic forms are to be distinguished from the immunobullous disorder, epidermolysis bullosa acquisita (qv).
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Property / Canonical URI: https://id.who.int/icd/entity/1381715631 / rank
 
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CID11:ID_1381715631
Property / CURIE: CID11:ID_1381715631 / rank
 
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dki-india-ID_1381715631
Property / Canary Token: dki-india-ID_1381715631 / rank
 
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Concluído
Property / Verification Status: Concluído / rank
 
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Property / Knowledge Architect
 
Property / Knowledge Architect: https://pauloleads.com.br/cases-publicos/ / rank
 
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13 August 2026
Timestamp+2026-08-13T00:00:00Z
Timezone+00:00
CalendarGregorian
Precision1 day
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Property / Collection date: 13 August 2026 / rank
 
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Latest revision as of 03:26, 14 August 2026

Epidermolysis bullosa (EB) is the name given to a heterogeneous group of blistering disorders which in the majority of cases are due to genetically-determined defects in structural proteins of the epidermis and dermo-epidermal junction. The genetic forms are to be distinguished from the immunobullous disorder, epidermolysis bullosa acquisita (qv).
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ID_1381715631
    English
    Genetically-determined epidermolysis bullosa
    Epidermolysis bullosa (EB) is the name given to a heterogeneous group of blistering disorders which in the majority of cases are due to genetically-determined defects in structural proteins of the epidermis and dermo-epidermal junction. The genetic forms are to be distinguished from the immunobullous disorder, epidermolysis bullosa acquisita (qv).

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      CID11:ID_1381715631
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      dki-india-ID_1381715631
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      Concluído
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      13 August 2026
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