733467001: Hereditary anetoderma (disorder)

SNOMED CT Concept\Clinical finding\...

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

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

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

\Disease\Genetic disease\Hereditary disease\Hereditary disorder by system\Hereditary disorder of the integument\Familial anetoderma
\Disease\Genetic disease\Hereditary disease\Autosomal hereditary disorder\Familial anetoderma
\Disease\Degenerative disorder\Degenerative skin disorder\Atrophic condition of skin\Anetoderma\Familial anetoderma
\Disease\Disorder of body system\Hereditary disorder by system\Hereditary disorder of the integument\Familial anetoderma
\Disease\Disorder of body system\Skin or mucosa lesion\Lesion of skin and/or skin-associated mucous membrane\Skin lesion\Anetoderma\Familial anetoderma
\Disease\Disorder of body system\Disorder of integument\Hereditary disorder of the integument\Familial anetoderma
\Disease\Disorder of body system\Disorder of integument\Disorder of skin and/or subcutaneous tissue\Disorder of skin\Degenerative skin disorder\Atrophic condition of skin\Anetoderma\Familial anetoderma
\Disease\Disorder of body system\Disorder of integument\Disorder of skin and/or subcutaneous tissue\Disorder of skin\Skin lesion\Anetoderma\Familial anetoderma
\Disease\Congenital disease\Familial anetoderma
\Disease\Disorder of soft tissue\Soft tissue lesion\Skin lesion\Anetoderma\Familial anetoderma
\Disease\Disorder of soft tissue\Disorder of skin and/or subcutaneous tissue\Disorder of skin\Degenerative skin disorder\Atrophic condition of skin\Anetoderma\Familial anetoderma
\Disease\Disorder of soft tissue\Disorder of skin and/or subcutaneous tissue\Disorder of skin\Skin lesion\Anetoderma\Familial anetoderma

Status: current, Primitive. Date: 31-Jul 2017. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module

2071471000168114 Familial anetoderma en Synonym Active Case insensitive SNOMED Clinical Terms Australian extension

3499490015 Hereditary anetoderma (disorder) en Fully specified name Active Case insensitive SNOMED CT core

3499491016 Hereditary macular atrophy en Synonym Active Case insensitive SNOMED CT core

3499492011 Hereditary anetoderma en Synonym Active Case insensitive 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 Case sensitive 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 Case sensitive SNOMED CT core

Expanded Value Set

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
Familial anetoderma	Associated morphology	Focal atrophy	true	Inferred relationship	Some	1
Familial anetoderma	Is a	Autosomal hereditary disorder	true	Inferred relationship	Some
Familial anetoderma	Is a	Congenital disease	true	Inferred relationship	Some
Familial anetoderma	Is a	Anetoderma	true	Inferred relationship	Some
Familial anetoderma	Is a	Hereditary disorder of the integument	true	Inferred relationship	Some
Familial anetoderma	Occurrence	Congenital	true	Inferred relationship	Some	1
Familial anetoderma	Finding site	Skin structure	true	Inferred relationship	Some	1

Inbound Relationships

Type

Active

Source

Characteristic

Refinability

Group

Reference Sets

Australian emergency department reference set

Clinical finding foundation reference set

Problem/Diagnosis reference set

Back to Start

Id	Description	Lang	Type	Status	Case?	Module
2071471000168114	Familial anetoderma	en	Synonym	Active	Case insensitive	SNOMED Clinical Terms Australian extension
3499490015	Hereditary anetoderma (disorder)	en	Fully specified name	Active	Case insensitive	SNOMED CT core
3499491016	Hereditary macular atrophy	en	Synonym	Active	Case insensitive	SNOMED CT core
3499492011	Hereditary anetoderma	en	Synonym	Active	Case insensitive	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	Case sensitive	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	Case sensitive	SNOMED CT core