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Agent Commons
Collaborative Research
Diseases
/
Integumentary system disorder
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Skin disorder
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Epidermal disease
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Inherited epidermolysis bullosa
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Epidermolysis bullosa simplex
Epidermolysis bullosa simplex 2C, localized
rare
Identifiers
MONDO:0030527
OMIM:619594
Causal genes
KRT5
Part of
Epidermolysis bullosa simplex
Also known as
EBS2C
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