733467001: Hereditary anetoderma (disorder)

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

\Skin AND/OR mucosa finding (finding)\Skin or mucosa lesion\Lesion of skin and/or skin-associated mucous membrane\Skin lesion\Anetoderma\Hereditary anetoderma (disorder)
\Skin AND/OR mucosa finding (finding)\Skin finding\Disorder of skin (disorder)\Degenerative skin disorder (disorder)\Atrophic condition of skin (disorder)\Anetoderma\Hereditary anetoderma (disorder)
\Skin AND/OR mucosa finding (finding)\Skin finding\Disorder of skin (disorder)\Skin lesion\Anetoderma\Hereditary anetoderma (disorder)

\General finding of soft tissue\Skin finding\Disorder of skin (disorder)\Degenerative skin disorder (disorder)\Atrophic condition of skin (disorder)\Anetoderma\Hereditary anetoderma (disorder)
\General finding of soft tissue\Skin finding\Disorder of skin (disorder)\Skin lesion\Anetoderma\Hereditary anetoderma (disorder)
\General finding of soft tissue\Disorder of soft tissue\Soft tissue lesion\Skin lesion\Anetoderma\Hereditary anetoderma (disorder)
\General finding of soft tissue\Disorder of soft tissue\Disorder of skin and/or subcutaneous tissue (disorder)\Disorder of skin (disorder)\Degenerative skin disorder (disorder)\Atrophic condition of skin (disorder)\Anetoderma\Hereditary anetoderma (disorder)
\General finding of soft tissue\Disorder of soft tissue\Disorder of skin and/or subcutaneous tissue (disorder)\Disorder of skin (disorder)\Skin lesion\Anetoderma\Hereditary anetoderma (disorder)

\Integumentary system finding\Disorder of integument\Hereditary disorder of the integument\Hereditary anetoderma (disorder)
\Integumentary system finding\Disorder of integument\Disorder of skin and/or subcutaneous tissue (disorder)\Disorder of skin (disorder)\Degenerative skin disorder (disorder)\Atrophic condition of skin (disorder)\Anetoderma\Hereditary anetoderma (disorder)
\Integumentary system finding\Disorder of integument\Disorder of skin and/or subcutaneous tissue (disorder)\Disorder of skin (disorder)\Skin lesion\Anetoderma\Hereditary anetoderma (disorder)
\Integumentary system finding\Skin finding\Disorder of skin (disorder)\Degenerative skin disorder (disorder)\Atrophic condition of skin (disorder)\Anetoderma\Hereditary anetoderma (disorder)
\Integumentary system finding\Skin finding\Disorder of skin (disorder)\Skin lesion\Anetoderma\Hereditary anetoderma (disorder)

\Disease\Genetic disease\Hereditary disease\Hereditary disorder by system\Hereditary disorder of the integument\Hereditary anetoderma (disorder)
\Disease\Genetic disease\Hereditary disease\Autosomal hereditary disorder\Hereditary anetoderma (disorder)
\Disease\Degenerative disorder\Atrophy (disorder)\Atrophic condition of skin (disorder)\Anetoderma\Hereditary anetoderma (disorder)
\Disease\Degenerative disorder\Degenerative skin disorder (disorder)\Atrophic condition of skin (disorder)\Anetoderma\Hereditary anetoderma (disorder)
\Disease\Disorder of body system\Hereditary disorder by system\Hereditary disorder of the integument\Hereditary anetoderma (disorder)
\Disease\Disorder of body system\Disorder of integument\Hereditary disorder of the integument\Hereditary anetoderma (disorder)
\Disease\Disorder of body system\Disorder of integument\Disorder of skin and/or subcutaneous tissue (disorder)\Disorder of skin (disorder)\Degenerative skin disorder (disorder)\Atrophic condition of skin (disorder)\Anetoderma\Hereditary anetoderma (disorder)
\Disease\Disorder of body system\Disorder of integument\Disorder of skin and/or subcutaneous tissue (disorder)\Disorder of skin (disorder)\Skin lesion\Anetoderma\Hereditary anetoderma (disorder)
\Disease\Congenital disease (disorder)\Hereditary anetoderma (disorder)
\Disease\Disorder of soft tissue\Soft tissue lesion\Skin lesion\Anetoderma\Hereditary anetoderma (disorder)
\Disease\Disorder of soft tissue\Disorder of skin and/or subcutaneous tissue (disorder)\Disorder of skin (disorder)\Degenerative skin disorder (disorder)\Atrophic condition of skin (disorder)\Anetoderma\Hereditary anetoderma (disorder)
\Disease\Disorder of soft tissue\Disorder of skin and/or subcutaneous tissue (disorder)\Disorder of skin (disorder)\Skin lesion\Anetoderma\Hereditary anetoderma (disorder)

Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jul 2017. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module

3499490015 Hereditary anetoderma (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core

3499491016 Hereditary macular atrophy en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core

3499492011 Hereditary anetoderma en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core

3500008013 An extremely rare genetic skin disease characterised by loss of elastin tissue leading to localised areas of flaccid skin and a family history of the disorder. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core

3500009017 An extremely rare genetic skin disease characterized by loss of elastin tissue leading to localized areas of flaccid skin and a family history of the disorder. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core

4012481000052111 ärftligt anetoderma 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 anetoderma (disorder)	Is a	Autosomal hereditary disorder	true	Inferred relationship	Some
Hereditary anetoderma (disorder)	Is a	Congenital disease (disorder)	true	Inferred relationship	Some
Hereditary anetoderma (disorder)	Is a	Anetoderma	true	Inferred relationship	Some
Hereditary anetoderma (disorder)	Is a	Hereditary disorder of the integument	true	Inferred relationship	Some
Hereditary anetoderma (disorder)	Occurrence	Congenital	true	Inferred relationship	Some	1
Hereditary anetoderma (disorder)	Finding site	Skin structure	true	Inferred relationship	Some	1
Hereditary anetoderma (disorder)	Associated morphology	Focal atrophy	true	Inferred relationship	Some	1

Inbound Relationships

Type

Active

Source

Characteristic

Refinability

Group

This concept is not in any reference sets

Back to Start

Id	Description	Lang	Type	Status	Case?	Module
3499490015	Hereditary anetoderma (disorder)	en	Fully specified name	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
3499491016	Hereditary macular atrophy	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
3499492011	Hereditary anetoderma	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
3500008013	An extremely rare genetic skin disease characterised by loss of elastin tissue leading to localised areas of flaccid skin and a family history of the disorder.	en	Definition	Active	Entire term case sensitive (core metadata concept)	SNOMED CT core
3500009017	An extremely rare genetic skin disease characterized by loss of elastin tissue leading to localized areas of flaccid skin and a family history of the disorder.	en	Definition	Active	Entire term case sensitive (core metadata concept)	SNOMED CT core
4012481000052111	ärftligt anetoderma	sv	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT Sweden NRC maintained module (core metadata concept)