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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
Epidermolytic hyperkeratosis 2A, autosomal dominant
rare
Identifiers
MONDO:0700248
OMIM:620150
Part of
Autosomal dominant epidermolytic ichthyosis
Epidermolytic hyperkeratosis 2
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