ONKI3 | Medical Subject Headings

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Epidermolysis Bullosa

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Hierarchy:	Medical Subject Headings (MeSH) ∟ Congenital, Hereditary, and Neonatal Diseases and Abnormalities ∟ Abnormalities ∟ Skin Abnormalities ∟ Epidermolysis Bullosa 37 coordinate concepts 4 subordinate concepts ∟ Epidermolysis Bullosa Acquisita \| ∟ Epidermolysis Bullosa Dystrophica \| ∟ Epidermolysis Bullosa Simplex \| ∟ Epidermolysis Bullosa, Junctional ∟ Acrodermatitis \| ∟ Dyskeratosis Congenita \| ∟ Ectodermal Dysplasia \| ∟ Ehlers-Danlos Syndrome \| ∟ Ichthyosis \| ∟ Incontinentia Pigmenti \| ∟ Port-Wine Stain \| ∟ Pseudoxanthoma Elasticum \| ∟ Rothmund-Thomson Syndrome \| ∟ Sclerema Neonatorum \| ∟ Xeroderma Pigmentosum \| ∟ Albinism \| ∟ Cutis Laxa \| ∟ Dermatitis, Atopic \| ∟ Ichthyosiform Erythroderma, Congenital \| ∟ Ichthyosis Bullosa of Siemens \| ∟ Ichthyosis Vulgaris \| ∟ Ichthyosis, X-Linked \| ∟ Keratoderma, Palmoplantar \| ∟ Keratosis Follicularis \| ∟ Leukokeratosis, Hereditary Mucosal \| ∟ Lipoid Proteinosis of Urbach and Wiethe \| ∟ Pemphigus, Benign Familial \| ∟ Porokeratosis \| ∟ Porphyria, Erythropoietic \| ∟ Porphyrias, Hepatic \| ∟ Sjogren-Larsson Syndrome \| ∟ Acantholysis \| ∟ Blister \| ∟ Dermatitis Herpetiformis \| ∟ Eczema, Dyshidrotic \| ∟ Erythema Multiforme \| ∟ Hydroa Vacciniforme \| ∟ Pemphigoid Gestationis \| ∟ Pemphigoid, Benign Mucous Membrane \| ∟ Pemphigoid, Bullous \| ∟ Pemphigus Medical Subject Headings (MeSH) ∟ Congenital, Hereditary, and Neonatal Diseases and Abnormalities ∟ Genetic Diseases, Inborn ∟ Skin Diseases, Genetic ∟ Epidermolysis Bullosa 37 coordinate concepts 4 subordinate concepts ∟ Epidermolysis Bullosa Acquisita \| ∟ Epidermolysis Bullosa Dystrophica \| ∟ Epidermolysis Bullosa Simplex \| ∟ Epidermolysis Bullosa, Junctional ∟ Acrodermatitis \| ∟ Dyskeratosis Congenita \| ∟ Ectodermal Dysplasia \| ∟ Ehlers-Danlos Syndrome \| ∟ Ichthyosis \| ∟ Incontinentia Pigmenti \| ∟ Port-Wine Stain \| ∟ Pseudoxanthoma Elasticum \| ∟ Rothmund-Thomson Syndrome \| ∟ Sclerema Neonatorum \| ∟ Xeroderma Pigmentosum \| ∟ Albinism \| ∟ Cutis Laxa \| ∟ Dermatitis, Atopic \| ∟ Ichthyosiform Erythroderma, Congenital \| ∟ Ichthyosis Bullosa of Siemens \| ∟ Ichthyosis Vulgaris \| ∟ Ichthyosis, X-Linked \| ∟ Keratoderma, Palmoplantar \| ∟ Keratosis Follicularis \| ∟ Leukokeratosis, Hereditary Mucosal \| ∟ Lipoid Proteinosis of Urbach and Wiethe \| ∟ Pemphigus, Benign Familial \| ∟ Porokeratosis \| ∟ Porphyria, Erythropoietic \| ∟ Porphyrias, Hepatic \| ∟ Sjogren-Larsson Syndrome \| ∟ Acantholysis \| ∟ Blister \| ∟ Dermatitis Herpetiformis \| ∟ Eczema, Dyshidrotic \| ∟ Erythema Multiforme \| ∟ Hydroa Vacciniforme \| ∟ Pemphigoid Gestationis \| ∟ Pemphigoid, Benign Mucous Membrane \| ∟ Pemphigoid, Bullous \| ∟ Pemphigus Medical Subject Headings (MeSH) ∟ Skin and Connective Tissue Diseases ∟ Skin Diseases ∟ Skin Abnormalities ∟ Epidermolysis Bullosa 37 coordinate concepts 4 subordinate concepts ∟ Epidermolysis Bullosa Acquisita \| ∟ Epidermolysis Bullosa Dystrophica \| ∟ Epidermolysis Bullosa Simplex \| ∟ Epidermolysis Bullosa, Junctional ∟ Acrodermatitis \| ∟ Dyskeratosis Congenita \| ∟ Ectodermal Dysplasia \| ∟ Ehlers-Danlos Syndrome \| ∟ Ichthyosis \| ∟ Incontinentia Pigmenti \| ∟ Port-Wine Stain \| ∟ Pseudoxanthoma Elasticum \| ∟ Rothmund-Thomson Syndrome \| ∟ Sclerema Neonatorum \| ∟ Xeroderma Pigmentosum \| ∟ Albinism \| ∟ Cutis Laxa \| ∟ Dermatitis, Atopic \| ∟ Ichthyosiform Erythroderma, Congenital \| ∟ Ichthyosis Bullosa of Siemens \| ∟ Ichthyosis Vulgaris \| ∟ Ichthyosis, X-Linked \| ∟ Keratoderma, Palmoplantar \| ∟ Keratosis Follicularis \| ∟ Leukokeratosis, Hereditary Mucosal \| ∟ Lipoid Proteinosis of Urbach and Wiethe \| ∟ Pemphigus, Benign Familial \| ∟ Porokeratosis \| ∟ Porphyria, Erythropoietic \| ∟ Porphyrias, Hepatic \| ∟ Sjogren-Larsson Syndrome \| ∟ Acantholysis \| ∟ Blister \| ∟ Dermatitis Herpetiformis \| ∟ Eczema, Dyshidrotic \| ∟ Erythema Multiforme \| ∟ Hydroa Vacciniforme \| ∟ Pemphigoid Gestationis \| ∟ Pemphigoid, Benign Mucous Membrane \| ∟ Pemphigoid, Bullous \| ∟ Pemphigus Medical Subject Headings (MeSH) ∟ Skin and Connective Tissue Diseases ∟ Skin Diseases ∟ Skin Diseases, Genetic ∟ Epidermolysis Bullosa 37 coordinate concepts 4 subordinate concepts ∟ Epidermolysis Bullosa Acquisita \| ∟ Epidermolysis Bullosa Dystrophica \| ∟ Epidermolysis Bullosa Simplex \| ∟ Epidermolysis Bullosa, Junctional ∟ Acrodermatitis \| ∟ Dyskeratosis Congenita \| ∟ Ectodermal Dysplasia \| ∟ Ehlers-Danlos Syndrome \| ∟ Ichthyosis \| ∟ Incontinentia Pigmenti \| ∟ Port-Wine Stain \| ∟ Pseudoxanthoma Elasticum \| ∟ Rothmund-Thomson Syndrome \| ∟ Sclerema Neonatorum \| ∟ Xeroderma Pigmentosum \| ∟ Albinism \| ∟ Cutis Laxa \| ∟ Dermatitis, Atopic \| ∟ Ichthyosiform Erythroderma, Congenital \| ∟ Ichthyosis Bullosa of Siemens \| ∟ Ichthyosis Vulgaris \| ∟ Ichthyosis, X-Linked \| ∟ Keratoderma, Palmoplantar \| ∟ Keratosis Follicularis \| ∟ Leukokeratosis, Hereditary Mucosal \| ∟ Lipoid Proteinosis of Urbach and Wiethe \| ∟ Pemphigus, Benign Familial \| ∟ Porokeratosis \| ∟ Porphyria, Erythropoietic \| ∟ Porphyrias, Hepatic \| ∟ Sjogren-Larsson Syndrome \| ∟ Acantholysis \| ∟ Blister \| ∟ Dermatitis Herpetiformis \| ∟ Eczema, Dyshidrotic \| ∟ Erythema Multiforme \| ∟ Hydroa Vacciniforme \| ∟ Pemphigoid Gestationis \| ∟ Pemphigoid, Benign Mucous Membrane \| ∟ Pemphigoid, Bullous \| ∟ Pemphigus Medical Subject Headings (MeSH) ∟ Skin and Connective Tissue Diseases ∟ Skin Diseases ∟ Skin Diseases, Vesiculobullous ∟ Epidermolysis Bullosa 37 coordinate concepts 4 subordinate concepts ∟ Epidermolysis Bullosa Acquisita \| ∟ Epidermolysis Bullosa Dystrophica \| ∟ Epidermolysis Bullosa Simplex \| ∟ Epidermolysis Bullosa, Junctional ∟ Acrodermatitis \| ∟ Dyskeratosis Congenita \| ∟ Ectodermal Dysplasia \| ∟ Ehlers-Danlos Syndrome \| ∟ Ichthyosis \| ∟ Incontinentia Pigmenti \| ∟ Port-Wine Stain \| ∟ Pseudoxanthoma Elasticum \| ∟ Rothmund-Thomson Syndrome \| ∟ Sclerema Neonatorum \| ∟ Xeroderma Pigmentosum \| ∟ Albinism \| ∟ Cutis Laxa \| ∟ Dermatitis, Atopic \| ∟ Ichthyosiform Erythroderma, Congenital \| ∟ Ichthyosis Bullosa of Siemens \| ∟ Ichthyosis Vulgaris \| ∟ Ichthyosis, X-Linked \| ∟ Keratoderma, Palmoplantar \| ∟ Keratosis Follicularis \| ∟ Leukokeratosis, Hereditary Mucosal \| ∟ Lipoid Proteinosis of Urbach and Wiethe \| ∟ Pemphigus, Benign Familial \| ∟ Porokeratosis \| ∟ Porphyria, Erythropoietic \| ∟ Porphyrias, Hepatic \| ∟ Sjogren-Larsson Syndrome \| ∟ Acantholysis \| ∟ Blister \| ∟ Dermatitis Herpetiformis \| ∟ Eczema, Dyshidrotic \| ∟ Erythema Multiforme \| ∟ Hydroa Vacciniforme \| ∟ Pemphigoid Gestationis \| ∟ Pemphigoid, Benign Mucous Membrane \| ∟ Pemphigoid, Bullous \| ∟ Pemphigus X
Broader terms:	Medical Subject Headings (MeSH) ∟ Congenital, Hereditary, and Neonatal Diseases and Abnormalities ∟ Abnormalities ∟ Skin Abnormalities ∟ Epidermolysis Bullosa Medical Subject Headings (MeSH) ∟ Congenital, Hereditary, and Neonatal Diseases and Abnormalities ∟ Genetic Diseases, Inborn ∟ Skin Diseases, Genetic ∟ Epidermolysis Bullosa Medical Subject Headings (MeSH) ∟ Skin and Connective Tissue Diseases ∟ Skin Diseases ∟ Skin Abnormalities ∟ Epidermolysis Bullosa Medical Subject Headings (MeSH) ∟ Skin and Connective Tissue Diseases ∟ Skin Diseases ∟ Skin Diseases, Genetic ∟ Epidermolysis Bullosa Medical Subject Headings (MeSH) ∟ Skin and Connective Tissue Diseases ∟ Skin Diseases ∟ Skin Diseases, Vesiculobullous ∟ Epidermolysis Bullosa Skin Abnormalities > Abnormalities > Congenital, Hereditary, and Neonatal Diseases and Abnormalities > Medical Subject Headings (MeSH) Skin Diseases, Genetic > Genetic Diseases, Inborn > Congenital, Hereditary, and Neonatal Diseases and Abnormalities > Medical Subject Headings (MeSH) Skin Abnormalities > 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) Skin Diseases, Vesiculobullous > Skin Diseases > Skin and Connective Tissue Diseases > Medical Subject Headings (MeSH) X
Narrower terms:	Epidermolysis Bullosa Acquisita \| Epidermolysis Bullosa Dystrophica \| Epidermolysis Bullosa Simplex \| Epidermolysis Bullosa, Junctional X
Annotation:	vesiculobullous skin dis; GEN only: prefer specifics; do not use /congen & do not coord with INFANT, NEWBORN, DISEASES X
Scope note:	Group of genetically determined disorders characterized by the blistering of skin and mucosae. There are four major forms: acquired, simple, junctional, and dystrophic. Each of the latter three has several varieties. 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:	Acrodermatitis \| Dyskeratosis Congenita \| Ectodermal Dysplasia \| Ehlers-Danlos Syndrome \| Ichthyosis \| Incontinentia Pigmenti \| Port-Wine Stain \| Pseudoxanthoma Elasticum \| Rothmund-Thomson Syndrome \| Sclerema Neonatorum \| Xeroderma Pigmentosum \| Albinism \| Cutis Laxa \| Dermatitis, Atopic \| Ichthyosiform Erythroderma, Congenital \| Ichthyosis Bullosa of Siemens \| Ichthyosis Vulgaris \| Ichthyosis, X-Linked \| Keratoderma, Palmoplantar \| Keratosis Follicularis \| Leukokeratosis, Hereditary Mucosal \| Lipoid Proteinosis of Urbach and Wiethe \| Pemphigus, Benign Familial \| Porokeratosis \| Porphyria, Erythropoietic \| Porphyrias, Hepatic \| Sjogren-Larsson Syndrome \| Acantholysis \| Blister \| Dermatitis Herpetiformis \| Eczema, Dyshidrotic \| Erythema Multiforme \| Hydroa Vacciniforme \| Pemphigoid Gestationis \| Pemphigoid, Benign Mucous Membrane \| Pemphigoid, Bullous \| Pemphigus X
URI:	X
Labels and equivalent concepts:	Ihon rakkulatauti (fi, replaced) Acantholysis Bullosa (en, replaced) Epidermolysis bullosa (la-FI, replaced) X
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