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716774008: Hereditary keratoacanthoma (disorder)

Status: current, Sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2020. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
3307520018 Hereditary keratoacanthoma (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
3307521019 Hereditary keratoacanthoma en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
3307522014 Familial keratoacanthoma en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
4696581013 Multiple familial keratoacanthoma en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
5401409014 A rare inherited skin cancer syndrome characterized by the coexistence of features typical of both multiple self-healing squamous epithelioma and generalized eruptive keratoacanthoma, such as multiple small miliary-type lesions, larger self-healing lesions, and nodulo-ulcerative lesions. Lesions do not have a predilection for the mucosal surfaces. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
5401410016 A rare inherited skin cancer syndrome characterised by the coexistence of features typical of both multiple self-healing squamous epithelioma and generalised eruptive keratoacanthoma, such as multiple small miliary-type lesions, larger self-healing lesions, and nodulo-ulcerative lesions. Lesions do not have a predilection for the mucosal surfaces. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
3307520018 Hereditary keratoacanthoma (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
3307520018 Hereditary keratoacanthoma (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
3307521019 Hereditary keratoacanthoma en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
3307521019 Hereditary keratoacanthoma en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
3307522014 Familial keratoacanthoma en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
3307522014 Familial keratoacanthoma en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
3307523016 Multiple keratoacanthoma en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
3307523016 Multiple keratoacanthoma en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
4696581013 Multiple familial keratoacanthoma en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
3307524010 A rare inherited skin cancer syndrome with the coexistence of features characteristic of both multiple keratoacanthoma, Ferguson Smith type and generalized eruptive keratoacanthoma, such as multiple small miliary-type lesions, larger self-healing lesions, and nodulo-ulcerative lesions. Lesions do not have a predilection for the mucosal surfaces. Transmission is autosomal dominant. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
3307525011 A rare inherited skin cancer syndrome with the coexistence of features characteristic of both multiple keratoacanthoma, Ferguson Smith type and generalised eruptive keratoacanthoma, such as multiple small miliary-type lesions, larger self-healing lesions, and nodulo-ulcerative lesions. Lesions do not have a predilection for the mucosal surfaces. Transmission is autosomal dominant. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
5401409014 A rare inherited skin cancer syndrome characterized by the coexistence of features typical of both multiple self-healing squamous epithelioma and generalized eruptive keratoacanthoma, such as multiple small miliary-type lesions, larger self-healing lesions, and nodulo-ulcerative lesions. Lesions do not have a predilection for the mucosal surfaces. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
5401410016 A rare inherited skin cancer syndrome characterised by the coexistence of features typical of both multiple self-healing squamous epithelioma and generalised eruptive keratoacanthoma, such as multiple small miliary-type lesions, larger self-healing lesions, and nodulo-ulcerative lesions. Lesions do not have a predilection for the mucosal surfaces. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
3425361001000113 Keratoakanthom, familiäres de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
6246011000241118 kératoacanthome familial multiple fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
6246021000241113 kératoacanthome héréditaire fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
6246031000241110 kératoacanthome familial fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
6246011000241118 kératoacanthome familial multiple fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
6246021000241113 kératoacanthome héréditaire fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
6246031000241110 kératoacanthome familial fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
3425361001000113 Keratoakanthom, familiäres de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module

0 descendants.

Expanded Value Set

Outbound Relationships Type Target Active Characteristic Refinability Group Values
A rare inherited skin cancer syndrome characterised by the coexistence of features typical of both multiple self-healing squamous epithelioma and generalised eruptive keratoacanthoma, such as multiple small miliary-type lesions, larger self-healing lesions, and nodulo-ulcerative lesions. Lesions do not have a predilection for the mucosal surfaces. Is a Autosomal dominant hereditary disorder true Inferred relationship Existential restriction modifier (core metadata concept)
A rare inherited skin cancer syndrome characterised by the coexistence of features typical of both multiple self-healing squamous epithelioma and generalised eruptive keratoacanthoma, such as multiple small miliary-type lesions, larger self-healing lesions, and nodulo-ulcerative lesions. Lesions do not have a predilection for the mucosal surfaces. Is a Keratoacanthoma (disorder) false Inferred relationship Existential restriction modifier (core metadata concept)
A rare inherited skin cancer syndrome characterised by the coexistence of features typical of both multiple self-healing squamous epithelioma and generalised eruptive keratoacanthoma, such as multiple small miliary-type lesions, larger self-healing lesions, and nodulo-ulcerative lesions. Lesions do not have a predilection for the mucosal surfaces. Is a Hereditary disorder of the integument (disorder) true Inferred relationship Existential restriction modifier (core metadata concept)
A rare inherited skin cancer syndrome characterised by the coexistence of features typical of both multiple self-healing squamous epithelioma and generalised eruptive keratoacanthoma, such as multiple small miliary-type lesions, larger self-healing lesions, and nodulo-ulcerative lesions. Lesions do not have a predilection for the mucosal surfaces. Is a Hereditary cancer-predisposing syndrome true Inferred relationship Existential restriction modifier (core metadata concept)
A rare inherited skin cancer syndrome characterised by the coexistence of features typical of both multiple self-healing squamous epithelioma and generalised eruptive keratoacanthoma, such as multiple small miliary-type lesions, larger self-healing lesions, and nodulo-ulcerative lesions. Lesions do not have a predilection for the mucosal surfaces. Associated morphology Keratoacanthoma - category false Inferred relationship Existential restriction modifier (core metadata concept) 1
A rare inherited skin cancer syndrome characterised by the coexistence of features typical of both multiple self-healing squamous epithelioma and generalised eruptive keratoacanthoma, such as multiple small miliary-type lesions, larger self-healing lesions, and nodulo-ulcerative lesions. Lesions do not have a predilection for the mucosal surfaces. Finding site Integumentary system structure false Inferred relationship Existential restriction modifier (core metadata concept) 1
A rare inherited skin cancer syndrome characterised by the coexistence of features typical of both multiple self-healing squamous epithelioma and generalised eruptive keratoacanthoma, such as multiple small miliary-type lesions, larger self-healing lesions, and nodulo-ulcerative lesions. Lesions do not have a predilection for the mucosal surfaces. Associated morphology Keratoacanthoma of uncertain behavior false Inferred relationship Existential restriction modifier (core metadata concept) 1
A rare inherited skin cancer syndrome characterised by the coexistence of features typical of both multiple self-healing squamous epithelioma and generalised eruptive keratoacanthoma, such as multiple small miliary-type lesions, larger self-healing lesions, and nodulo-ulcerative lesions. Lesions do not have a predilection for the mucosal surfaces. Finding site Skin structure of multiple topographic sites (body structure) true Inferred relationship Existential restriction modifier (core metadata concept) 1
A rare inherited skin cancer syndrome characterised by the coexistence of features typical of both multiple self-healing squamous epithelioma and generalised eruptive keratoacanthoma, such as multiple small miliary-type lesions, larger self-healing lesions, and nodulo-ulcerative lesions. Lesions do not have a predilection for the mucosal surfaces. Is a Multiple keratoacanthoma of skin (disorder) true Inferred relationship Existential restriction modifier (core metadata concept)
A rare inherited skin cancer syndrome characterised by the coexistence of features typical of both multiple self-healing squamous epithelioma and generalised eruptive keratoacanthoma, such as multiple small miliary-type lesions, larger self-healing lesions, and nodulo-ulcerative lesions. Lesions do not have a predilection for the mucosal surfaces. Associated morphology Malignant keratoacanthoma true Inferred relationship Existential restriction modifier (core metadata concept) 1
Inbound Relationships Type Active Source Characteristic Refinability Group

Reference Sets

Component annotation with string value reference set (foundation metadata concept)

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