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\Hereditary anetoderma
\Skin AND/OR mucosa finding\Skin finding\Disorder of skin\Degenerative skin disorder\Atrophic condition of skin\Anetoderma\Hereditary anetoderma
\Skin AND/OR mucosa finding\Skin finding\Disorder of skin\Skin lesion\Anetoderma\Hereditary anetoderma

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

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

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

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

Descriptions:

Id Description Lang Type Status Case? Module

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

3499491016 Hereditary macular atrophy en Synonym Active Entire term case insensitive SNOMED CT core module

3499492011 Hereditary anetoderma en Synonym Active Entire term case insensitive SNOMED CT core module

Expanded Value Set

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

Inbound Relationships

Type

Active

Source

Characteristic

Refinability

Group

This concept is not in any reference sets

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Id	Description	Lang	Type	Status	Case?	Module
3499490015	Hereditary anetoderma (disorder)	en	Fully specified name	Active	Entire term case insensitive	SNOMED CT core module
3499491016	Hereditary macular atrophy	en	Synonym	Active	Entire term case insensitive	SNOMED CT core module
3499492011	Hereditary anetoderma	en	Synonym	Active	Entire term case insensitive	SNOMED CT core module