ONKI3 | Medical Subject Headings

The ONKI is provided as a part of the ONKI Living Lab - an open lab for testing the latest semantic web technologies in practice, with real users like you. Currently, over 10 000 people are using ONKI each month.

We hope you like the ONKI service and enjoy using it for your purposes!

If you encounter any problems or have improvement ideas, please contact the ONKI team. We are also very much interested in your success stories in using ONKI - please share your experiences!

The ONKI Team

Jouni Tuominen, Living Lab contact person, APIs, widgets, publishing of ontologies, etc.
Eero Hyvönen, professor, head of research group

Former members: Kim Viljanen, Rami Alatalo.

Building the future of the Semantic Web and beyond.

SeCo's homepage
For the latest semantic news, follow us on Twitter and fan us on Facebook!

How can we help you?

Live presentations about ONKI: what it is? how to use it?
Support for creating and publishing ontologies.
Online technical support for using ONKI.
Co-operation in projects.
And more, please ask.

suomeksi på svenska in English

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

The way concept relations are shown: separately in hierarchy

Hyperkeratosis, Epidermolytic

Loading results...


Hierarchy:	Medical Subject Headings (MeSH) ∟ Congenital, Hereditary, and Neonatal Diseases and Abnormalities ∟ Abnormalities ∟ Skin Abnormalities ∟ Ichthyosis ∟ Ichthyosiform Erythroderma, Congenital ∟ Hyperkeratosis, Epidermolytic 1 coordinate concept ∟ Ichthyosis, Lamellar Medical Subject Headings (MeSH) ∟ Congenital, Hereditary, and Neonatal Diseases and Abnormalities ∟ Genetic Diseases, Inborn ∟ Skin Diseases, Genetic ∟ Ichthyosiform Erythroderma, Congenital ∟ Hyperkeratosis, Epidermolytic 1 coordinate concept ∟ Ichthyosis, Lamellar Medical Subject Headings (MeSH) ∟ Congenital, Hereditary, and Neonatal Diseases and Abnormalities ∟ Infant, Newborn, Diseases ∟ Ichthyosis ∟ Ichthyosiform Erythroderma, Congenital ∟ Hyperkeratosis, Epidermolytic 1 coordinate concept ∟ Ichthyosis, Lamellar Medical Subject Headings (MeSH) ∟ Skin and Connective Tissue Diseases ∟ Skin Diseases ∟ Keratosis ∟ Ichthyosis ∟ Ichthyosiform Erythroderma, Congenital ∟ Hyperkeratosis, Epidermolytic 1 coordinate concept ∟ Ichthyosis, Lamellar Medical Subject Headings (MeSH) ∟ Skin and Connective Tissue Diseases ∟ Skin Diseases ∟ Skin Abnormalities ∟ Ichthyosis ∟ Ichthyosiform Erythroderma, Congenital ∟ Hyperkeratosis, Epidermolytic 1 coordinate concept ∟ Ichthyosis, Lamellar Medical Subject Headings (MeSH) ∟ Skin and Connective Tissue Diseases ∟ Skin Diseases ∟ Skin Diseases, Genetic ∟ Ichthyosiform Erythroderma, Congenital ∟ Hyperkeratosis, Epidermolytic 1 coordinate concept ∟ Ichthyosis, Lamellar X
Broader terms:	Medical Subject Headings (MeSH) ∟ Congenital, Hereditary, and Neonatal Diseases and Abnormalities ∟ Abnormalities ∟ Skin Abnormalities ∟ Ichthyosis ∟ Ichthyosiform Erythroderma, Congenital ∟ Hyperkeratosis, Epidermolytic Medical Subject Headings (MeSH) ∟ Congenital, Hereditary, and Neonatal Diseases and Abnormalities ∟ Genetic Diseases, Inborn ∟ Skin Diseases, Genetic ∟ Ichthyosiform Erythroderma, Congenital ∟ Hyperkeratosis, Epidermolytic Medical Subject Headings (MeSH) ∟ Congenital, Hereditary, and Neonatal Diseases and Abnormalities ∟ Infant, Newborn, Diseases ∟ Ichthyosis ∟ Ichthyosiform Erythroderma, Congenital ∟ Hyperkeratosis, Epidermolytic Medical Subject Headings (MeSH) ∟ Skin and Connective Tissue Diseases ∟ Skin Diseases ∟ Keratosis ∟ Ichthyosis ∟ Ichthyosiform Erythroderma, Congenital ∟ Hyperkeratosis, Epidermolytic Medical Subject Headings (MeSH) ∟ Skin and Connective Tissue Diseases ∟ Skin Diseases ∟ Skin Abnormalities ∟ Ichthyosis ∟ Ichthyosiform Erythroderma, Congenital ∟ Hyperkeratosis, Epidermolytic Medical Subject Headings (MeSH) ∟ Skin and Connective Tissue Diseases ∟ Skin Diseases ∟ Skin Diseases, Genetic ∟ Ichthyosiform Erythroderma, Congenital ∟ Hyperkeratosis, Epidermolytic Ichthyosiform Erythroderma, Congenital > Ichthyosis > Skin Abnormalities > Abnormalities > Congenital, Hereditary, and Neonatal Diseases and Abnormalities > Medical Subject Headings (MeSH) Ichthyosiform Erythroderma, Congenital > Skin Diseases, Genetic > Genetic Diseases, Inborn > Congenital, Hereditary, and Neonatal Diseases and Abnormalities > Medical Subject Headings (MeSH) Ichthyosiform Erythroderma, Congenital > Ichthyosis > Infant, Newborn, Diseases > Congenital, Hereditary, and Neonatal Diseases and Abnormalities > Medical Subject Headings (MeSH) Ichthyosiform Erythroderma, Congenital > Ichthyosis > Keratosis > Skin Diseases > Skin and Connective Tissue Diseases > Medical Subject Headings (MeSH) Ichthyosiform Erythroderma, Congenital > Ichthyosis > Skin Abnormalities > Skin Diseases > Skin and Connective Tissue Diseases > Medical Subject Headings (MeSH) Ichthyosiform Erythroderma, Congenital > Skin Diseases, Genetic > Skin Diseases > Skin and Connective Tissue Diseases > Medical Subject Headings (MeSH) X
History note:	Ichthyosiform Erythroderma, Congenital (1991-1992) \| Ichthyosis (1966-1992) \| Keratosis (1972-1992) \| Skin Diseases, Vesiculobullous (1972-1992)X
historyNote*:	1993(1979); use ICHTHYOSIFORM ERYTHRODERMA, CONGENITAL 1991-1992; for ERYTHRODERMA ICHTHYOSIFORME, BULLOUS use ICHTHYOSIFORM ERYTHRODERMA, CONGENITAL 1991-1992, use SKIN DISEASES, BULLOUS 1979-1990 X
publicMeSHNote*:	1993; see ICHTHYOSIFORM ERYTHRODERMA, CONGENITAL 1991-1992; for ERYTHRODERMA ICHTHYOSIFORME, BULLOUS see ICHTHYOSIFORM ERYTHRODERMA, CONGENITAL 1991-1992, see SKIN DISEASES, BULLOUS 1979-1990 X
Scope note:	A form of congenital ichthyosis inherited as an autosomal dominant trait and characterized by ERYTHRODERMA and severe hyperkeratosis. It is manifested at birth by blisters followed by the appearance of thickened, horny, verruciform scales over the entire body, but accentuated in flexural areas. Mutations in the genes that encode KERATIN-1 and KERATIN-10 have been associated with this disorder. X
activeMeSHYear*:	2007X
dateCreated*:	1992-05-20X
dateEstablished*:	1993-01-01X
dateRevised*:	2006-07-05X
recordAuthorizer*:	sjnX
recordMaintainer*:	jmpX
recordOriginator*:	PLSX
Type:	Concept X
Coordinate terms:	Ichthyosis, Lamellar X
URI:	X
Labels and equivalent concepts:	Epidermolyyttinen hyperkeratoosi (fi) Hyperkeratoosi, epidermolyyttinen (fi, replaced) Ichthyosiform Erythroderma, Bullous Congenital (en, replaced) Erythroderma Ichthyosiforme, Bullous (en, replaced) Congenital Bullous Ichthyosiform Erythroderma (en, replaced) Congenital Ichthyosiform Erythroderma, Bullous (en, replaced) Bullous Congenital Ichthyosiform Erythroderma (en, replaced) Hyperkeratosis epidermolytica (la-FI, replaced) X
Share:	X