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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 Reference Sets
3307520018 Hereditary keratoacanthoma (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core GB English: Preferred (foundation metadata concept)
3307521019 Hereditary keratoacanthoma en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core GB English: Preferred (foundation metadata concept)
3307522014 Familial keratoacanthoma en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core GB English: Acceptable (foundation metadata concept)
3307523016 Multiple keratoacanthoma en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core GB English: Acceptable (foundation metadata concept)
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 US English: Preferred (foundation metadata concept)
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 GB English: Preferred (foundation metadata concept)

0 descendants.

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 Keratoacanthoma - category (morphologic abnormality) true Inferred relationship Some 1
Hereditary keratoacanthoma (disorder) Finding site Structure of integumentary system (body structure) true Inferred relationship Some 1

Inbound Relationships Type Active Source Characteristic Refinability Group

Reference Sets

Description inactivation indicator reference set

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