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

Keratosis Follicularis

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Hierarchy:	Medical Subject Headings (MeSH) ∟ Congenital, Hereditary, and Neonatal Diseases and Abnormalities ∟ Genetic Diseases, Inborn ∟ Skin Diseases, Genetic ∟ Keratosis Follicularis 28 coordinate concepts ∟ 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 \| ∟ Keratoderma, Palmoplantar \| ∟ 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 ∟ Keratosis Follicularis 28 coordinate concepts ∟ 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 \| ∟ Keratoderma, Palmoplantar \| ∟ 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 ∟ Keratosis Follicularis 28 coordinate concepts ∟ 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 \| ∟ Keratoderma, Palmoplantar \| ∟ 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 ∟ Keratosis Follicularis Medical Subject Headings (MeSH) ∟ Skin and Connective Tissue Diseases ∟ Skin Diseases ∟ Keratosis ∟ Keratosis Follicularis Medical Subject Headings (MeSH) ∟ Skin and Connective Tissue Diseases ∟ Skin Diseases ∟ Skin Diseases, Genetic ∟ Keratosis Follicularis 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
Scope note:	A slowly progressive autosomal dominant disorder of keratinization characterized by pinkish-to-tan papules that coalesce to form plaques. These lesions become darker over time and commonly fuse, forming papillomatous and warty malodorous growths. X
activeMeSHYear*:	2002 \| 2003 \| 2004 \| 2005 \| 2006 \| 2007X
dateCreated*:	1999-01-01X
dateRevised*:	2001-07-25X
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 \| Keratoderma, Palmoplantar \| 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:	Follikulaarinen keratoosi (fi) Follikulaarinen sarveistuma (fi, replaced) Follikulaarinen dyskeratoosi (fi, replaced) Darierin tauti (fi, replaced) Darier's Disease (en, replaced) Darier Disease (en, replaced) Dyskeratosis follicularis (la-FI, replaced) Keratosis follicularis (la-FI, replaced) Morbus Darier (la-FI, replaced) X
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