ONKI3 | Medical Subject Headings

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Ichthyosis Vulgaris

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Hierarchy:	Medical Subject Headings (MeSH) ∟ Congenital, Hereditary, and Neonatal Diseases and Abnormalities ∟ Abnormalities ∟ Skin Abnormalities ∟ Ichthyosis ∟ Ichthyosis Vulgaris 23 coordinate concepts ∟ Albinism \| ∟ Cutis Laxa \| ∟ Dermatitis, Atopic \| ∟ Dyskeratosis Congenita \| ∟ Ectodermal Dysplasia \| ∟ Ehlers-Danlos Syndrome \| ∟ Epidermolysis Bullosa \| ∟ Ichthyosiform Erythroderma, Congenital \| ∟ Ichthyosis Bullosa of Siemens \| ∟ Ichthyosis, X-Linked \| ∟ Incontinentia Pigmenti \| ∟ Keratoderma, Palmoplantar \| ∟ 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 Medical Subject Headings (MeSH) ∟ Congenital, Hereditary, and Neonatal Diseases and Abnormalities ∟ Genetic Diseases, Inborn ∟ Skin Diseases, Genetic ∟ Ichthyosis Vulgaris 23 coordinate concepts ∟ Albinism \| ∟ Cutis Laxa \| ∟ Dermatitis, Atopic \| ∟ Dyskeratosis Congenita \| ∟ Ectodermal Dysplasia \| ∟ Ehlers-Danlos Syndrome \| ∟ Epidermolysis Bullosa \| ∟ Ichthyosiform Erythroderma, Congenital \| ∟ Ichthyosis Bullosa of Siemens \| ∟ Ichthyosis, X-Linked \| ∟ Incontinentia Pigmenti \| ∟ Keratoderma, Palmoplantar \| ∟ 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 Medical Subject Headings (MeSH) ∟ Congenital, Hereditary, and Neonatal Diseases and Abnormalities ∟ Infant, Newborn, Diseases ∟ Ichthyosis ∟ Ichthyosis Vulgaris 23 coordinate concepts ∟ Albinism \| ∟ Cutis Laxa \| ∟ Dermatitis, Atopic \| ∟ Dyskeratosis Congenita \| ∟ Ectodermal Dysplasia \| ∟ Ehlers-Danlos Syndrome \| ∟ Epidermolysis Bullosa \| ∟ Ichthyosiform Erythroderma, Congenital \| ∟ Ichthyosis Bullosa of Siemens \| ∟ Ichthyosis, X-Linked \| ∟ Incontinentia Pigmenti \| ∟ Keratoderma, Palmoplantar \| ∟ 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 Medical Subject Headings (MeSH) ∟ Skin and Connective Tissue Diseases ∟ Skin Diseases ∟ Keratosis ∟ Ichthyosis ∟ Ichthyosis Vulgaris 23 coordinate concepts ∟ Albinism \| ∟ Cutis Laxa \| ∟ Dermatitis, Atopic \| ∟ Dyskeratosis Congenita \| ∟ Ectodermal Dysplasia \| ∟ Ehlers-Danlos Syndrome \| ∟ Epidermolysis Bullosa \| ∟ Ichthyosiform Erythroderma, Congenital \| ∟ Ichthyosis Bullosa of Siemens \| ∟ Ichthyosis, X-Linked \| ∟ Incontinentia Pigmenti \| ∟ Keratoderma, Palmoplantar \| ∟ 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 Medical Subject Headings (MeSH) ∟ Skin and Connective Tissue Diseases ∟ Skin Diseases ∟ Skin Abnormalities ∟ Ichthyosis ∟ Ichthyosis Vulgaris 23 coordinate concepts ∟ Albinism \| ∟ Cutis Laxa \| ∟ Dermatitis, Atopic \| ∟ Dyskeratosis Congenita \| ∟ Ectodermal Dysplasia \| ∟ Ehlers-Danlos Syndrome \| ∟ Epidermolysis Bullosa \| ∟ Ichthyosiform Erythroderma, Congenital \| ∟ Ichthyosis Bullosa of Siemens \| ∟ Ichthyosis, X-Linked \| ∟ Incontinentia Pigmenti \| ∟ Keratoderma, Palmoplantar \| ∟ 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 Medical Subject Headings (MeSH) ∟ Skin and Connective Tissue Diseases ∟ Skin Diseases ∟ Skin Diseases, Genetic ∟ Ichthyosis Vulgaris 23 coordinate concepts ∟ Albinism \| ∟ Cutis Laxa \| ∟ Dermatitis, Atopic \| ∟ Dyskeratosis Congenita \| ∟ Ectodermal Dysplasia \| ∟ Ehlers-Danlos Syndrome \| ∟ Epidermolysis Bullosa \| ∟ Ichthyosiform Erythroderma, Congenital \| ∟ Ichthyosis Bullosa of Siemens \| ∟ Ichthyosis, X-Linked \| ∟ Incontinentia Pigmenti \| ∟ Keratoderma, Palmoplantar \| ∟ 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 X
Broader terms:	Medical Subject Headings (MeSH) ∟ Congenital, Hereditary, and Neonatal Diseases and Abnormalities ∟ Abnormalities ∟ Skin Abnormalities ∟ Ichthyosis ∟ Ichthyosis Vulgaris Medical Subject Headings (MeSH) ∟ Congenital, Hereditary, and Neonatal Diseases and Abnormalities ∟ Genetic Diseases, Inborn ∟ Skin Diseases, Genetic ∟ Ichthyosis Vulgaris Medical Subject Headings (MeSH) ∟ Congenital, Hereditary, and Neonatal Diseases and Abnormalities ∟ Infant, Newborn, Diseases ∟ Ichthyosis ∟ Ichthyosis Vulgaris Medical Subject Headings (MeSH) ∟ Skin and Connective Tissue Diseases ∟ Skin Diseases ∟ Keratosis ∟ Ichthyosis ∟ Ichthyosis Vulgaris Medical Subject Headings (MeSH) ∟ Skin and Connective Tissue Diseases ∟ Skin Diseases ∟ Skin Abnormalities ∟ Ichthyosis ∟ Ichthyosis Vulgaris Medical Subject Headings (MeSH) ∟ Skin and Connective Tissue Diseases ∟ Skin Diseases ∟ Skin Diseases, Genetic ∟ Ichthyosis Vulgaris Ichthyosis > 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) Ichthyosis > Infant, Newborn, Diseases > Congenital, Hereditary, and Neonatal Diseases and Abnormalities > Medical Subject Headings (MeSH) Ichthyosis > Keratosis > Skin Diseases > Skin and Connective Tissue Diseases > Medical Subject Headings (MeSH) Ichthyosis > 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
Annotation:	do not use /congen & do not coord with INFANT, NEWBORN, DISEASES X
History note:	Ichthyosis (1966-1990)X
historyNote*:	91 X
publicMeSHNote*:	91 X
Scope note:	Most common form of ICHTHYOSIS characterized by prominent scaling especially on the exterior surfaces of the extremities. It is inherited as an autosomal dominant trait. X
activeMeSHYear*:	2002 \| 2003 \| 2004 \| 2005 \| 2006 \| 2007X
dateCreated*:	1990-02-12X
dateEstablished*:	1991-01-01X
dateRevised*:	2001-07-25X
recordAuthorizer*:	sjnX
recordMaintainer*:	nnsX
recordOriginator*:	AGSX
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, X-Linked \| Incontinentia Pigmenti \| Keratoderma, Palmoplantar \| 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 X
URI:	X
Labels and equivalent concepts:	Yleinen kalansuomutauti (fi) Yleinen autosomaalinen kalansuomutauti (fi, replaced) Tavallinen iktyoosi (fi, replaced) Tavallinen kalansuomutauti (fi, replaced) Fiskfjällssjuka (sv) Ichthyosis vulgaris (sv, replaced) Ichthyosis Vulgaris, Dominant (en, replaced) Ichthyosis vulgaris (la-FI, replaced) Ichthyosis congenita vulgaris (la-FI, replaced) X
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