716774008: Hereditary keratoacanthoma (disorder)

SNOMED CT Concept\Clinical finding (finding)\...

\Mass of body structure\Neoplasm of integumentary system (disorder)\Keratoacanthoma\Hereditary keratoacanthoma (disorder)

\Integumentary system finding\Disorder of integument\...

\Neoplasm of integumentary system (disorder)\Keratoacanthoma\Hereditary keratoacanthoma (disorder)

\Hereditary disorder of the integument\Hereditary keratoacanthoma (disorder)

\Disease\Genetic disease\Hereditary disease\Hereditary cancer-predisposing syndrome\Hereditary keratoacanthoma (disorder)
\Disease\Genetic disease\Hereditary disease\Hereditary disorder by system\Hereditary disorder of the integument\Hereditary keratoacanthoma (disorder)
\Disease\Genetic disease\Hereditary disease\Autosomal hereditary disorder\Autosomal dominant hereditary disorder\Hereditary keratoacanthoma (disorder)
\Disease\Neoplasm and/or hamartoma (disorder)\Neoplastic disease\Neoplasm of integumentary system (disorder)\Keratoacanthoma\Hereditary keratoacanthoma (disorder)
\Disease\Neoplasm and/or hamartoma (disorder)\Neoplastic disease\Neoplastic disease of uncertain behavior\Keratoacanthoma\Hereditary keratoacanthoma (disorder)
\Disease\Disorder of body system\Hereditary disorder by system\Hereditary disorder of the integument\Hereditary keratoacanthoma (disorder)
\Disease\Disorder of body system\Disorder of integument\Neoplasm of integumentary system (disorder)\Keratoacanthoma\Hereditary keratoacanthoma (disorder)
\Disease\Disorder of body system\Disorder of integument\Hereditary disorder of the integument\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

3307523016 Multiple 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

3868461000052117 hereditärt keratoakantom sv Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Sweden NRC maintained module (core metadata concept)

Expanded Value Set

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
Hereditary keratoacanthoma (disorder)	Is a	Autosomal dominant hereditary disorder	true	Inferred relationship	Some
Hereditary keratoacanthoma (disorder)	Is a	Keratoacanthoma	true	Inferred relationship	Some
Hereditary keratoacanthoma (disorder)	Is a	Hereditary disorder of the integument	true	Inferred relationship	Some
Hereditary keratoacanthoma (disorder)	Is a	Hereditary cancer-predisposing syndrome	true	Inferred relationship	Some
Hereditary keratoacanthoma (disorder)	Associated morphology	keratoakantom, kategori	false	Inferred relationship	Some	1
Hereditary keratoacanthoma (disorder)	Finding site	Structure of integumentary system (body structure)	true	Inferred relationship	Some	1
Hereditary keratoacanthoma (disorder)	Associated morphology	Keratoacanthoma of uncertain behavior (morphologic abnormality)	true	Inferred relationship	Some	1

Inbound Relationships

Type

Active

Source

Characteristic

Refinability

Group

Reference Sets

Description inactivation indicator reference set

Back to Start

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
3307523016	Multiple 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
3868461000052117	hereditärt keratoakantom	sv	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT Sweden NRC maintained module (core metadata concept)