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Ectodermal Dysplasia

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Hierarchy:	Medical Subject Headings (MeSH) ∟ Congenital, Hereditary, and Neonatal Diseases and Abnormalities ∟ Abnormalities ∟ Abnormalities, Multiple ∟ Ectodermal Dysplasia 58 coordinate concepts 7 subordinate concepts ∟ Ectodermal Dysplasia 1, Anhidrotic \| ∟ Ectodermal Dysplasia 3, Anhidrotic \| ∟ Ectodermal Dysplasia, Hypohidrotic, Autosomal Recessive \| ∟ Ellis-Van Creveld Syndrome \| ∟ Focal Dermal Hypoplasia \| ∟ Neurocutaneous Syndromes \| ∟ Pachyonychia Congenita ∟ Acrodermatitis \| ∟ Dyskeratosis Congenita \| ∟ Ehlers-Danlos Syndrome \| ∟ Epidermolysis Bullosa \| ∟ 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 \| ∟ Alagille Syndrome \| ∟ Angelman Syndrome \| ∟ Bardet-Biedl Syndrome \| ∟ Basal Cell Nevus Syndrome \| ∟ Beckwith-Wiedemann Syndrome \| ∟ Bloom Syndrome \| ∟ Branchio-Oto-Renal Syndrome \| ∟ Cockayne Syndrome \| ∟ Cri-du-Chat Syndrome \| ∟ De Lange Syndrome \| ∟ Down Syndrome \| ∟ Gardner Syndrome \| ∟ Holoprosencephaly \| ∟ Laurence-Moon Syndrome \| ∟ LEOPARD Syndrome \| ∟ Marfan Syndrome \| ∟ Mobius Syndrome \| ∟ Nail-Patella Syndrome \| ∟ Oculocerebrorenal Syndrome \| ∟ Orofaciodigital Syndromes \| ∟ POEMS Syndrome \| ∟ Prader-Willi Syndrome \| ∟ Proteus Syndrome \| ∟ Prune Belly Syndrome \| ∟ Rubella Syndrome, Congenital \| ∟ Rubinstein-Taybi Syndrome \| ∟ Short Rib-Polydactyly Syndrome \| ∟ Smith-Lemli-Opitz Syndrome \| ∟ Waardenburg's Syndrome \| ∟ Wolfram Syndrome \| ∟ Zellweger Syndrome Medical Subject Headings (MeSH) ∟ Congenital, Hereditary, and Neonatal Diseases and Abnormalities ∟ Abnormalities ∟ Skin Abnormalities ∟ Ectodermal Dysplasia 58 coordinate concepts 7 subordinate concepts ∟ Ectodermal Dysplasia 1, Anhidrotic \| ∟ Ectodermal Dysplasia 3, Anhidrotic \| ∟ Ectodermal Dysplasia, Hypohidrotic, Autosomal Recessive \| ∟ Ellis-Van Creveld Syndrome \| ∟ Focal Dermal Hypoplasia \| ∟ Neurocutaneous Syndromes \| ∟ Pachyonychia Congenita ∟ Acrodermatitis \| ∟ Dyskeratosis Congenita \| ∟ Ehlers-Danlos Syndrome \| ∟ Epidermolysis Bullosa \| ∟ 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 \| ∟ Alagille Syndrome \| ∟ Angelman Syndrome \| ∟ Bardet-Biedl Syndrome \| ∟ Basal Cell Nevus Syndrome \| ∟ Beckwith-Wiedemann Syndrome \| ∟ Bloom Syndrome \| ∟ Branchio-Oto-Renal Syndrome \| ∟ Cockayne Syndrome \| ∟ Cri-du-Chat Syndrome \| ∟ De Lange Syndrome \| ∟ Down Syndrome \| ∟ Gardner Syndrome \| ∟ Holoprosencephaly \| ∟ Laurence-Moon Syndrome \| ∟ LEOPARD Syndrome \| ∟ Marfan Syndrome \| ∟ Mobius Syndrome \| ∟ Nail-Patella Syndrome \| ∟ Oculocerebrorenal Syndrome \| ∟ Orofaciodigital Syndromes \| ∟ POEMS Syndrome \| ∟ Prader-Willi Syndrome \| ∟ Proteus Syndrome \| ∟ Prune Belly Syndrome \| ∟ Rubella Syndrome, Congenital \| ∟ Rubinstein-Taybi Syndrome \| ∟ Short Rib-Polydactyly Syndrome \| ∟ Smith-Lemli-Opitz Syndrome \| ∟ Waardenburg's Syndrome \| ∟ Wolfram Syndrome \| ∟ Zellweger Syndrome Medical Subject Headings (MeSH) ∟ Congenital, Hereditary, and Neonatal Diseases and Abnormalities ∟ Genetic Diseases, Inborn ∟ Skin Diseases, Genetic ∟ Ectodermal Dysplasia 58 coordinate concepts 7 subordinate concepts ∟ Ectodermal Dysplasia 1, Anhidrotic \| ∟ Ectodermal Dysplasia 3, Anhidrotic \| ∟ Ectodermal Dysplasia, Hypohidrotic, Autosomal Recessive \| ∟ Ellis-Van Creveld Syndrome \| ∟ Focal Dermal Hypoplasia \| ∟ Neurocutaneous Syndromes \| ∟ Pachyonychia Congenita ∟ Acrodermatitis \| ∟ Dyskeratosis Congenita \| ∟ Ehlers-Danlos Syndrome \| ∟ Epidermolysis Bullosa \| ∟ 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 \| ∟ Alagille Syndrome \| ∟ Angelman Syndrome \| ∟ Bardet-Biedl Syndrome \| ∟ Basal Cell Nevus Syndrome \| ∟ Beckwith-Wiedemann Syndrome \| ∟ Bloom Syndrome \| ∟ Branchio-Oto-Renal Syndrome \| ∟ Cockayne Syndrome \| ∟ Cri-du-Chat Syndrome \| ∟ De Lange Syndrome \| ∟ Down Syndrome \| ∟ Gardner Syndrome \| ∟ Holoprosencephaly \| ∟ Laurence-Moon Syndrome \| ∟ LEOPARD Syndrome \| ∟ Marfan Syndrome \| ∟ Mobius Syndrome \| ∟ Nail-Patella Syndrome \| ∟ Oculocerebrorenal Syndrome \| ∟ Orofaciodigital Syndromes \| ∟ POEMS Syndrome \| ∟ Prader-Willi Syndrome \| ∟ Proteus Syndrome \| ∟ Prune Belly Syndrome \| ∟ Rubella Syndrome, Congenital \| ∟ Rubinstein-Taybi Syndrome \| ∟ Short Rib-Polydactyly Syndrome \| ∟ Smith-Lemli-Opitz Syndrome \| ∟ Waardenburg's Syndrome \| ∟ Wolfram Syndrome \| ∟ Zellweger Syndrome Medical Subject Headings (MeSH) ∟ Skin and Connective Tissue Diseases ∟ Skin Diseases ∟ Skin Abnormalities ∟ Ectodermal Dysplasia 58 coordinate concepts 7 subordinate concepts ∟ Ectodermal Dysplasia 1, Anhidrotic \| ∟ Ectodermal Dysplasia 3, Anhidrotic \| ∟ Ectodermal Dysplasia, Hypohidrotic, Autosomal Recessive \| ∟ Ellis-Van Creveld Syndrome \| ∟ Focal Dermal Hypoplasia \| ∟ Neurocutaneous Syndromes \| ∟ Pachyonychia Congenita ∟ Acrodermatitis \| ∟ Dyskeratosis Congenita \| ∟ Ehlers-Danlos Syndrome \| ∟ Epidermolysis Bullosa \| ∟ 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 \| ∟ Alagille Syndrome \| ∟ Angelman Syndrome \| ∟ Bardet-Biedl Syndrome \| ∟ Basal Cell Nevus Syndrome \| ∟ Beckwith-Wiedemann Syndrome \| ∟ Bloom Syndrome \| ∟ Branchio-Oto-Renal Syndrome \| ∟ Cockayne Syndrome \| ∟ Cri-du-Chat Syndrome \| ∟ De Lange Syndrome \| ∟ Down Syndrome \| ∟ Gardner Syndrome \| ∟ Holoprosencephaly \| ∟ Laurence-Moon Syndrome \| ∟ LEOPARD Syndrome \| ∟ Marfan Syndrome \| ∟ Mobius Syndrome \| ∟ Nail-Patella Syndrome \| ∟ Oculocerebrorenal Syndrome \| ∟ Orofaciodigital Syndromes \| ∟ POEMS Syndrome \| ∟ Prader-Willi Syndrome \| ∟ Proteus Syndrome \| ∟ Prune Belly Syndrome \| ∟ Rubella Syndrome, Congenital \| ∟ Rubinstein-Taybi Syndrome \| ∟ Short Rib-Polydactyly Syndrome \| ∟ Smith-Lemli-Opitz Syndrome \| ∟ Waardenburg's Syndrome \| ∟ Wolfram Syndrome \| ∟ Zellweger Syndrome Medical Subject Headings (MeSH) ∟ Skin and Connective Tissue Diseases ∟ Skin Diseases ∟ Skin Diseases, Genetic ∟ Ectodermal Dysplasia 58 coordinate concepts 7 subordinate concepts ∟ Ectodermal Dysplasia 1, Anhidrotic \| ∟ Ectodermal Dysplasia 3, Anhidrotic \| ∟ Ectodermal Dysplasia, Hypohidrotic, Autosomal Recessive \| ∟ Ellis-Van Creveld Syndrome \| ∟ Focal Dermal Hypoplasia \| ∟ Neurocutaneous Syndromes \| ∟ Pachyonychia Congenita ∟ Acrodermatitis \| ∟ Dyskeratosis Congenita \| ∟ Ehlers-Danlos Syndrome \| ∟ Epidermolysis Bullosa \| ∟ 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 \| ∟ Alagille Syndrome \| ∟ Angelman Syndrome \| ∟ Bardet-Biedl Syndrome \| ∟ Basal Cell Nevus Syndrome \| ∟ Beckwith-Wiedemann Syndrome \| ∟ Bloom Syndrome \| ∟ Branchio-Oto-Renal Syndrome \| ∟ Cockayne Syndrome \| ∟ Cri-du-Chat Syndrome \| ∟ De Lange Syndrome \| ∟ Down Syndrome \| ∟ Gardner Syndrome \| ∟ Holoprosencephaly \| ∟ Laurence-Moon Syndrome \| ∟ LEOPARD Syndrome \| ∟ Marfan Syndrome \| ∟ Mobius Syndrome \| ∟ Nail-Patella Syndrome \| ∟ Oculocerebrorenal Syndrome \| ∟ Orofaciodigital Syndromes \| ∟ POEMS Syndrome \| ∟ Prader-Willi Syndrome \| ∟ Proteus Syndrome \| ∟ Prune Belly Syndrome \| ∟ Rubella Syndrome, Congenital \| ∟ Rubinstein-Taybi Syndrome \| ∟ Short Rib-Polydactyly Syndrome \| ∟ Smith-Lemli-Opitz Syndrome \| ∟ Waardenburg's Syndrome \| ∟ Wolfram Syndrome \| ∟ Zellweger Syndrome X
Broader terms:	Medical Subject Headings (MeSH) ∟ Congenital, Hereditary, and Neonatal Diseases and Abnormalities ∟ Abnormalities ∟ Abnormalities, Multiple ∟ Ectodermal Dysplasia Medical Subject Headings (MeSH) ∟ Congenital, Hereditary, and Neonatal Diseases and Abnormalities ∟ Abnormalities ∟ Skin Abnormalities ∟ Ectodermal Dysplasia Medical Subject Headings (MeSH) ∟ Congenital, Hereditary, and Neonatal Diseases and Abnormalities ∟ Genetic Diseases, Inborn ∟ Skin Diseases, Genetic ∟ Ectodermal Dysplasia Medical Subject Headings (MeSH) ∟ Skin and Connective Tissue Diseases ∟ Skin Diseases ∟ Skin Abnormalities ∟ Ectodermal Dysplasia Medical Subject Headings (MeSH) ∟ Skin and Connective Tissue Diseases ∟ Skin Diseases ∟ Skin Diseases, Genetic ∟ Ectodermal Dysplasia Abnormalities, Multiple > Abnormalities > Congenital, Hereditary, and Neonatal Diseases and Abnormalities > Medical Subject Headings (MeSH) 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) X
Narrower terms:	Ectodermal Dysplasia 1, Anhidrotic \| Ectodermal Dysplasia 3, Anhidrotic \| Ectodermal Dysplasia, Hypohidrotic, Autosomal Recessive \| Ellis-Van Creveld Syndrome \| Focal Dermal Hypoplasia \| Neurocutaneous Syndromes \| Pachyonychia Congenita X
historyNote*:	1965 X
publicMeSHNote*:	1965; ECTODERMAL DEFECT, CONGENITAL was heading 1963-1986 X
Scope note:	A group of hereditary disorders involving tissues and structures derived from the embryonic ectoderm. They are characterized by the presence of abnormalities at birth and involvement of both the epidermis and skin appendages. They are generally nonprogressive and diffuse. Various forms exist, including anhidrotic and hidrotic dysplasias, FOCAL DERMAL HYPOPLASIA, and aplasia cutis congenita. X
activeMeSHYear*:	2007X
dateCreated*:	1999-01-01X
dateEstablished*:	1965-01-01X
dateRevised*:	2006-07-05X
recordAuthorizer*:	sjnX
recordMaintainer*:	jmpX
recordOriginator*:	NLMX
Type:	Concept X
Coordinate terms:	Acrodermatitis \| Dyskeratosis Congenita \| Ehlers-Danlos Syndrome \| Epidermolysis Bullosa \| 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 \| Alagille Syndrome \| Angelman Syndrome \| Bardet-Biedl Syndrome \| Basal Cell Nevus Syndrome \| Beckwith-Wiedemann Syndrome \| Bloom Syndrome \| Branchio-Oto-Renal Syndrome \| Cockayne Syndrome \| Cri-du-Chat Syndrome \| De Lange Syndrome \| Down Syndrome \| Gardner Syndrome \| Holoprosencephaly \| Laurence-Moon Syndrome \| LEOPARD Syndrome \| Marfan Syndrome \| Mobius Syndrome \| Nail-Patella Syndrome \| Oculocerebrorenal Syndrome \| Orofaciodigital Syndromes \| POEMS Syndrome \| Prader-Willi Syndrome \| Proteus Syndrome \| Prune Belly Syndrome \| Rubella Syndrome, Congenital \| Rubinstein-Taybi Syndrome \| Short Rib-Polydactyly Syndrome \| Smith-Lemli-Opitz Syndrome \| Waardenburg's Syndrome \| Wolfram Syndrome \| Zellweger Syndrome X
URI:	X
Labels and equivalent concepts:	Ektodermaalinen dysplasia (fi) Ektodermal dysplasi (sv) Anhidrotisk ektodermal dysplasi (sv, replaced) Christ-Siemens-Touraine syndrom (sv, replaced) Hypohidrotisk ektodermal dysplasi (sv, replaced) Hydrotic Ectodermal Dysplasia (en, replaced) Ectodermal Defect, Congenital (en, replaced) Clouston's Syndrome (en, replaced) Congenital Ectodermal Defect (en, replaced) Defect, Congenital Ectodermal (en, replaced) Anhydrotic Ectodermal Dysplasia (en, replaced) Dysplasia ectodermalis (la-FI, replaced) X
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