Epidermolysis bullosa simplex with mottled pigmentation (Q106961): Difference between revisions
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Revision as of 13:57, 17 August 2026
Epidermolysis bullosa simplex with mottled pigmentation (EBS-MP) is an autosomal dominant basal subtype of EBS due to mutations in the KRT5 gene which encodes keratin 5. It is characterised by generalised blistering with mottled or reticulate brown pigmentation.
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | ID_1688797966 |
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| English | Epidermolysis bullosa simplex with mottled pigmentation |
Epidermolysis bullosa simplex with mottled pigmentation (EBS-MP) is an autosomal dominant basal subtype of EBS due to mutations in the KRT5 gene which encodes keratin 5. It is characterised by generalised blistering with mottled or reticulate brown pigmentation. |
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CID11:ID_1688797966
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dki-india-ID_1688797966
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Concluído
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