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Diseases / Disorder of development or morphogenesis/ Keratinization disease/ Epidermolytic ichthyosis

Autosomal dominant epidermolytic ichthyosis

rare

Identifiers: MONDO:0020702 Orphanet:312
Part of: Autosomal dominant disease Epidermolytic ichthyosis

Subtypes

All diseases Rare only

Disease Rare Not rare Subtypes

Annular epidermolytic ichthyosis MONDO:0011870 2
Epidermolytic hyperkeratosis 2A, autosomal dominant MONDO:0700248

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