ONKI3 | Medical Subject Headings

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The way concept relations are shown: separately in hierarchy

Keratoderma, Palmoplantar, Epidermolytic

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Hierarchy:	Medical Subject Headings (MeSH) ∟ Congenital, Hereditary, and Neonatal Diseases and Abnormalities ∟ Genetic Diseases, Inborn ∟ Skin Diseases, Genetic ∟ Keratoderma, Palmoplantar ∟ Keratoderma, Palmoplantar, Diffuse ∟ Keratoderma, Palmoplantar, Epidermolytic Medical Subject Headings (MeSH) ∟ Skin and Connective Tissue Diseases ∟ Skin Diseases ∟ Keratosis ∟ Keratoderma, Palmoplantar ∟ Keratoderma, Palmoplantar, Diffuse ∟ Keratoderma, Palmoplantar, Epidermolytic Medical Subject Headings (MeSH) ∟ Skin and Connective Tissue Diseases ∟ Skin Diseases ∟ Skin Diseases, Genetic ∟ Keratoderma, Palmoplantar ∟ Keratoderma, Palmoplantar, Diffuse ∟ Keratoderma, Palmoplantar, Epidermolytic X
Broader terms:	Medical Subject Headings (MeSH) ∟ Congenital, Hereditary, and Neonatal Diseases and Abnormalities ∟ Genetic Diseases, Inborn ∟ Skin Diseases, Genetic ∟ Keratoderma, Palmoplantar ∟ Keratoderma, Palmoplantar, Diffuse ∟ Keratoderma, Palmoplantar, Epidermolytic Medical Subject Headings (MeSH) ∟ Skin and Connective Tissue Diseases ∟ Skin Diseases ∟ Keratosis ∟ Keratoderma, Palmoplantar ∟ Keratoderma, Palmoplantar, Diffuse ∟ Keratoderma, Palmoplantar, Epidermolytic Medical Subject Headings (MeSH) ∟ Skin and Connective Tissue Diseases ∟ Skin Diseases ∟ Skin Diseases, Genetic ∟ Keratoderma, Palmoplantar ∟ Keratoderma, Palmoplantar, Diffuse ∟ Keratoderma, Palmoplantar, Epidermolytic Keratoderma, Palmoplantar, Diffuse > Keratoderma, Palmoplantar > Skin Diseases, Genetic > Genetic Diseases, Inborn > Congenital, Hereditary, and Neonatal Diseases and Abnormalities > Medical Subject Headings (MeSH) Keratoderma, Palmoplantar, Diffuse > Keratoderma, Palmoplantar > Keratosis > Skin Diseases > Skin and Connective Tissue Diseases > Medical Subject Headings (MeSH) Keratoderma, Palmoplantar, Diffuse > Keratoderma, Palmoplantar > Skin Diseases, Genetic > Skin Diseases > Skin and Connective Tissue Diseases > Medical Subject Headings (MeSH) X
History note:	Keratoderma, Palmoplantar, Diffuse (1989-2006)X
historyNote*:	2007 X
publicMeSHNote*:	2007 X
Scope note:	An autosomal dominant hereditary skin disease characterized by epidermolytic hyperkeratosis that is strictly confined to the palms and soles. It has been associated with mutations in the gene that codes for KERATIN-9. X
activeMeSHYear*:	2007X
dateCreated*:	2006-07-05X
dateEstablished*:	2007-01-01X
recordAuthorizer*:	sjnX
recordMaintainer*:	jmpX
recordOriginator*:	jmpX
Type:	Concept X
URI:	X
Labels and equivalent concepts:	Epidermolyyttinen palmoplantaarinen keratoderma (fi) Unna-Thost Disease, Epidermolytic (en, replaced) Thost-Unna Disease, Epidermolytic (en, replaced) EPPK (Epidermolytic Palmoplantar Keratoderma) (en, replaced) X
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