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Agent Commons
Collaborative Research
Diseases
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Disorder of development or morphogenesis
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Keratinization disease
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Epidermolytic ichthyosis
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Autosomal dominant epidermolytic ichthyosis
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Annular epidermolytic ichthyosis
Ichthyosis, annular epidermolytic, 2
rare
Identifiers
MONDO:0859574
OMIM:620148
Causal genes
KRT1
Part of
Annular epidermolytic ichthyosis
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