ONKI3 | Medical Subject Headings

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The way property values are displayed: value/row values side by side

The way concept relations are shown: separately in hierarchy

Papillon-Lefevre Disease

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Hierarchy:	Medical Subject Headings (MeSH) ∟ Congenital, Hereditary, and Neonatal Diseases and Abnormalities ∟ Genetic Diseases, Inborn ∟ Skin Diseases, Genetic ∟ Keratoderma, Palmoplantar ∟ Papillon-Lefevre Disease 1 coordinate concept ∟ Keratoderma, Palmoplantar, Diffuse Medical Subject Headings (MeSH) ∟ Skin and Connective Tissue Diseases ∟ Skin Diseases ∟ Keratosis ∟ Keratoderma, Palmoplantar ∟ Papillon-Lefevre Disease 1 coordinate concept ∟ Keratoderma, Palmoplantar, Diffuse Medical Subject Headings (MeSH) ∟ Skin and Connective Tissue Diseases ∟ Skin Diseases ∟ Skin Diseases, Genetic ∟ Keratoderma, Palmoplantar ∟ Papillon-Lefevre Disease 1 coordinate concept ∟ Keratoderma, Palmoplantar, Diffuse X
Broader terms:	Medical Subject Headings (MeSH) ∟ Congenital, Hereditary, and Neonatal Diseases and Abnormalities ∟ Genetic Diseases, Inborn ∟ Skin Diseases, Genetic ∟ Keratoderma, Palmoplantar ∟ Papillon-Lefevre Disease Medical Subject Headings (MeSH) ∟ Skin and Connective Tissue Diseases ∟ Skin Diseases ∟ Keratosis ∟ Keratoderma, Palmoplantar ∟ Papillon-Lefevre Disease Medical Subject Headings (MeSH) ∟ Skin and Connective Tissue Diseases ∟ Skin Diseases ∟ Skin Diseases, Genetic ∟ Keratoderma, Palmoplantar ∟ Papillon-Lefevre Disease Keratoderma, Palmoplantar > Skin Diseases, Genetic > Genetic Diseases, Inborn > Congenital, Hereditary, and Neonatal Diseases and Abnormalities > Medical Subject Headings (MeSH) Keratoderma, Palmoplantar > Keratosis > Skin Diseases > Skin and Connective Tissue Diseases > Medical Subject Headings (MeSH) Keratoderma, Palmoplantar > Skin Diseases, Genetic > Skin Diseases > Skin and Connective Tissue Diseases > Medical Subject Headings (MeSH) X
Annotation:	palmoplantar keratoderma with periodontitis X
historyNote*:	91(75); was see under KERATOSIS PALMARIS ET PLANTARIS 1975-90 (which became KERATODERMA, PALMOPLANTAR 1993) X
onlineNote*:	search KERATODERMA, PALMOPLANTAR 1974 X
publicMeSHNote*:	91; was see under KERATOSIS PALMARIS ET PLANTARIS 1975-90 (which became KERATODERMA, PALMOPLANTAR 1993) X
Scope note:	Rare, autosomal recessive disorder occurring between the first and fifth years of life. It is characterized by palmoplantar keratoderma with periodontitis followed by the premature shedding of both deciduous and permanent teeth. X
activeMeSHYear*:	2002 \| 2003 \| 2004 \| 2005 \| 2006 \| 2007X
dateCreated*:	1999-01-01X
dateEstablished*:	1991-01-01X
dateRevised*:	2001-07-25X
recordAuthorizer*:	sjnX
recordMaintainer*:	nnsX
recordOriginator*:	NLMX
Type:	Concept X
Coordinate terms:	Keratoderma, Palmoplantar, Diffuse X
URI:	X
Labels and equivalent concepts:	Papillon-Lèfevren tauti (fi) Synnynnäinen kämmenen ja jalkapohjan keratoosi (fi, replaced) Synnynnäinen kämmen-jalkapohjakeratoosi (fi, replaced) Papillon-Lèfevren oireyhtymä (fi, replaced) Papillon-Lèfevren syndrooma (fi, replaced) Papillon-Lefevres sjukdom (sv) Papillon-Lefevre Syndrome (en, replaced) Morbus Papillon-Lèfevre (la-FI, replaced) Syndroma Papillon-Lèfevre (la-FI, replaced) X
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