ONKI3 | Medical Subject Headings

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Keratoderma, Palmoplantar

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Hierarchy:	Medical Subject Headings (MeSH) ∟ Congenital, Hereditary, and Neonatal Diseases and Abnormalities ∟ Genetic Diseases, Inborn ∟ Skin Diseases, Genetic ∟ Keratoderma, Palmoplantar 28 coordinate concepts 2 subordinate concepts ∟ Keratoderma, Palmoplantar, Diffuse \| ∟ Papillon-Lefevre Disease ∟ Albinism \| ∟ Cutis Laxa \| ∟ Dermatitis, Atopic \| ∟ Dyskeratosis Congenita \| ∟ Ectodermal Dysplasia \| ∟ Ehlers-Danlos Syndrome \| ∟ Epidermolysis Bullosa \| ∟ Ichthyosiform Erythroderma, Congenital \| ∟ Ichthyosis Bullosa of Siemens \| ∟ Ichthyosis Vulgaris \| ∟ Ichthyosis, X-Linked \| ∟ Incontinentia Pigmenti \| ∟ Keratosis Follicularis \| ∟ Leukokeratosis, Hereditary Mucosal \| ∟ Lipoid Proteinosis of Urbach and Wiethe \| ∟ Pemphigus, Benign Familial \| ∟ Porokeratosis \| ∟ Porphyria, Erythropoietic \| ∟ Porphyrias, Hepatic \| ∟ Pseudoxanthoma Elasticum \| ∟ Rothmund-Thomson Syndrome \| ∟ Sjogren-Larsson Syndrome \| ∟ Xeroderma Pigmentosum \| ∟ Callosities \| ∟ Cholesteatoma \| ∟ Ichthyosis \| ∟ Keratosis, Seborrheic \| ∟ Parakeratosis Medical Subject Headings (MeSH) ∟ Skin and Connective Tissue Diseases ∟ Skin Diseases ∟ Keratosis ∟ Keratoderma, Palmoplantar 28 coordinate concepts 2 subordinate concepts ∟ Keratoderma, Palmoplantar, Diffuse \| ∟ Papillon-Lefevre Disease ∟ Albinism \| ∟ Cutis Laxa \| ∟ Dermatitis, Atopic \| ∟ Dyskeratosis Congenita \| ∟ Ectodermal Dysplasia \| ∟ Ehlers-Danlos Syndrome \| ∟ Epidermolysis Bullosa \| ∟ Ichthyosiform Erythroderma, Congenital \| ∟ Ichthyosis Bullosa of Siemens \| ∟ Ichthyosis Vulgaris \| ∟ Ichthyosis, X-Linked \| ∟ Incontinentia Pigmenti \| ∟ Keratosis Follicularis \| ∟ Leukokeratosis, Hereditary Mucosal \| ∟ Lipoid Proteinosis of Urbach and Wiethe \| ∟ Pemphigus, Benign Familial \| ∟ Porokeratosis \| ∟ Porphyria, Erythropoietic \| ∟ Porphyrias, Hepatic \| ∟ Pseudoxanthoma Elasticum \| ∟ Rothmund-Thomson Syndrome \| ∟ Sjogren-Larsson Syndrome \| ∟ Xeroderma Pigmentosum \| ∟ Callosities \| ∟ Cholesteatoma \| ∟ Ichthyosis \| ∟ Keratosis, Seborrheic \| ∟ Parakeratosis Medical Subject Headings (MeSH) ∟ Skin and Connective Tissue Diseases ∟ Skin Diseases ∟ Skin Diseases, Genetic ∟ Keratoderma, Palmoplantar 28 coordinate concepts 2 subordinate concepts ∟ Keratoderma, Palmoplantar, Diffuse \| ∟ Papillon-Lefevre Disease ∟ Albinism \| ∟ Cutis Laxa \| ∟ Dermatitis, Atopic \| ∟ Dyskeratosis Congenita \| ∟ Ectodermal Dysplasia \| ∟ Ehlers-Danlos Syndrome \| ∟ Epidermolysis Bullosa \| ∟ Ichthyosiform Erythroderma, Congenital \| ∟ Ichthyosis Bullosa of Siemens \| ∟ Ichthyosis Vulgaris \| ∟ Ichthyosis, X-Linked \| ∟ Incontinentia Pigmenti \| ∟ Keratosis Follicularis \| ∟ Leukokeratosis, Hereditary Mucosal \| ∟ Lipoid Proteinosis of Urbach and Wiethe \| ∟ Pemphigus, Benign Familial \| ∟ Porokeratosis \| ∟ Porphyria, Erythropoietic \| ∟ Porphyrias, Hepatic \| ∟ Pseudoxanthoma Elasticum \| ∟ Rothmund-Thomson Syndrome \| ∟ Sjogren-Larsson Syndrome \| ∟ Xeroderma Pigmentosum \| ∟ Callosities \| ∟ Cholesteatoma \| ∟ Ichthyosis \| ∟ Keratosis, Seborrheic \| ∟ Parakeratosis X
Broader terms:	Medical Subject Headings (MeSH) ∟ Congenital, Hereditary, and Neonatal Diseases and Abnormalities ∟ Genetic Diseases, Inborn ∟ Skin Diseases, Genetic ∟ Keratoderma, Palmoplantar Medical Subject Headings (MeSH) ∟ Skin and Connective Tissue Diseases ∟ Skin Diseases ∟ Keratosis ∟ Keratoderma, Palmoplantar Medical Subject Headings (MeSH) ∟ Skin and Connective Tissue Diseases ∟ Skin Diseases ∟ Skin Diseases, Genetic ∟ Keratoderma, Palmoplantar Skin Diseases, Genetic > Genetic Diseases, Inborn > Congenital, Hereditary, and Neonatal Diseases and Abnormalities > Medical Subject Headings (MeSH) Keratosis > Skin Diseases > Skin and Connective Tissue Diseases > Medical Subject Headings (MeSH) Skin Diseases, Genetic > Skin Diseases > Skin and Connective Tissue Diseases > Medical Subject Headings (MeSH) X
Narrower terms:	Keratoderma, Palmoplantar, Diffuse \| Papillon-Lefevre Disease X
Annotation:	do not confuse with KERATODERMA, PALMOPLANTAR, DIFFUSE or with POROKERATOSIS PALMARIS ET PLANTARIS DISSEMINATA see POROKERATOSIS; note X-ref HYPERKERATOSIS PALMARIS ET PLANTARIS X
historyNote*:	93; was KERATOSIS PALMARIS ET PLANTARIS 1974-92; KERATODERMA, PALMOPLANTAR was see KERATOSIS PALMARIS ET PLANTARIS 1990-92 X
onlineNote*:	use KERATODERMA, PALMOPLANTAR to search KERATOSIS PALMARIS ET PLANTARIS 1974-92 X
publicMeSHNote*:	93; was KERATOSIS PALMARIS ET PLANTARIS 1974-92; KERATODERMA, PALMOPLANTAR was see KERATOSIS PALMARIS ET PLANTARIS 1990-92 X
Scope note:	Group of mostly hereditary disorders characterized by thickening of the palms and soles as a result of excessive keratin formation leading to hypertrophy of the stratum corneum (hyperkeratosis). X
activeMeSHYear*:	2007X
dateCreated*:	1999-01-01X
dateEstablished*:	1974-01-01X
dateRevised*:	2006-07-05X
recordAuthorizer*:	sjnX
recordMaintainer*:	nnsX
recordOriginator*:	NLMX
Type:	Concept X
Coordinate terms:	Albinism \| Cutis Laxa \| Dermatitis, Atopic \| Dyskeratosis Congenita \| Ectodermal Dysplasia \| Ehlers-Danlos Syndrome \| Epidermolysis Bullosa \| Ichthyosiform Erythroderma, Congenital \| Ichthyosis Bullosa of Siemens \| Ichthyosis Vulgaris \| Ichthyosis, X-Linked \| Incontinentia Pigmenti \| Keratosis Follicularis \| Leukokeratosis, Hereditary Mucosal \| Lipoid Proteinosis of Urbach and Wiethe \| Pemphigus, Benign Familial \| Porokeratosis \| Porphyria, Erythropoietic \| Porphyrias, Hepatic \| Pseudoxanthoma Elasticum \| Rothmund-Thomson Syndrome \| Sjogren-Larsson Syndrome \| Xeroderma Pigmentosum \| Callosities \| Cholesteatoma \| Ichthyosis \| Keratosis, Seborrheic \| Parakeratosis X
URI:	X
Labels and equivalent concepts:	Palmoplantaarinen keratoderma (fi) Käden ja jalan sarveisihoisuus (fi, replaced) Palmoplantar keratoderma (sv, replaced) Palmoplantar Keratoderma (en, replaced) Keratosis Palmaris et Plantaris (en, replaced) Keratosis, Palmoplantar (en, replaced) Hyperkeratosis Palmaris et Plantaris (en, replaced) Keratoderma palmoplantare (la-FI, replaced) Keratosis punctata (la-FI, replaced) X
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