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

Epidermolytic hyperkeratosis 2

rare

Identifiers: MONDO:0958184
Causal genes: KRT10
Part of: Epidermolytic ichthyosis

Subtypes

All diseases Rare only

Disease

Epidermolytic hyperkeratosis 2A, autosomal dominant MONDO:0700248
Epidermolytic hyperkeratosis 2B, autosomal recessive MONDO:0700245
Ichthyosis, annular epidermolytic 1 MONDO:0100303

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