716774008: Hereditary keratoacanthoma (disorder)

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

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

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	false	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	Keratoacanthoma - category	false	Inferred relationship	Some	1
Hereditary keratoacanthoma (disorder)	Finding site	Structure of integumentary system (body structure)	false	Inferred relationship	Some	1
Hereditary keratoacanthoma (disorder)	Associated morphology	Keratoacanthoma of uncertain behavior	false	Inferred relationship	Some	1
Hereditary keratoacanthoma (disorder)	Finding site	Skin structure of multiple topographic sites (body structure)	true	Inferred relationship	Some	1
Hereditary keratoacanthoma (disorder)	Is a	Multiple keratoacanthoma of skin (disorder)	true	Inferred relationship	Some
Hereditary keratoacanthoma (disorder)	Associated morphology	Malignant keratoacanthoma	true	Inferred relationship	Some	1

Inbound Relationships

Characteristic

Refinability

Reference Sets

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
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