403774004: Hereditary sclerosing poikiloderma of Weary (disorder)

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

\Skin AND/OR mucosa finding (finding)\Skin finding\Disorder of skin (disorder)\Degenerative skin disorder (disorder)\Atrophic condition of skin (disorder)\Poikiloderma (disorder)\Hereditary sclerosing poikiloderma\Hereditary sclerosing poikiloderma of Weary (disorder)

\General finding of soft tissue\Skin finding\Disorder of skin (disorder)\Degenerative skin disorder (disorder)\Atrophic condition of skin (disorder)\Poikiloderma (disorder)\Hereditary sclerosing poikiloderma\Hereditary sclerosing poikiloderma of Weary (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)\Poikiloderma (disorder)\Hereditary sclerosing poikiloderma\Hereditary sclerosing poikiloderma of Weary (disorder)

\Integumentary system finding\Disorder of integument\Hereditary disorder of the integument (disorder)\Hereditary sclerosing poikiloderma\Hereditary sclerosing poikiloderma of Weary (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)\Poikiloderma (disorder)\Hereditary sclerosing poikiloderma\Hereditary sclerosing poikiloderma of Weary (disorder)
\Integumentary system finding\Skin finding\Disorder of skin (disorder)\Degenerative skin disorder (disorder)\Atrophic condition of skin (disorder)\Poikiloderma (disorder)\Hereditary sclerosing poikiloderma\Hereditary sclerosing poikiloderma of Weary (disorder)

\Disease\Genetic disease\Hereditary disease\Hereditary disorder by system (disorder)\Hereditary disorder of the integument (disorder)\Hereditary sclerosing poikiloderma\Hereditary sclerosing poikiloderma of Weary (disorder)
\Disease\Degenerative disorder\Degenerative skin disorder (disorder)\Atrophic condition of skin (disorder)\Poikiloderma (disorder)\Hereditary sclerosing poikiloderma\Hereditary sclerosing poikiloderma of Weary (disorder)
\Disease\Disorder of body system\Hereditary disorder by system (disorder)\Hereditary disorder of the integument (disorder)\Hereditary sclerosing poikiloderma\Hereditary sclerosing poikiloderma of Weary (disorder)
\Disease\Disorder of body system\Disorder of integument\Hereditary disorder of the integument (disorder)\Hereditary sclerosing poikiloderma\Hereditary sclerosing poikiloderma of Weary (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)\Poikiloderma (disorder)\Hereditary sclerosing poikiloderma\Hereditary sclerosing poikiloderma of Weary (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)\Poikiloderma (disorder)\Hereditary sclerosing poikiloderma\Hereditary sclerosing poikiloderma of Weary (disorder)

Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jul 2003. Module: SNOMED CT core

Descriptions:

Expanded Value Set

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
Hereditary sclerosing poikiloderma of Weary (disorder)	Is a	poïkilodermie avec syndrome génétique ou congénital	false	Inferred relationship	Existential restriction modifier (core metadata concept)
Hereditary sclerosing poikiloderma of Weary (disorder)	Associated morphology	dégénérescence	false	Inferred relationship	Existential restriction modifier (core metadata concept)
Hereditary sclerosing poikiloderma of Weary (disorder)	Associated morphology	Telangiectasis	false	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Hereditary sclerosing poikiloderma of Weary (disorder)	Finding site	Microscopic skin vascular structure (body structure)	false	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Hereditary sclerosing poikiloderma of Weary (disorder)	Occurrence	Congenital	false	Inferred relationship	Existential restriction modifier (core metadata concept)	3
Hereditary sclerosing poikiloderma of Weary (disorder)	Finding site	Skin structure	false	Inferred relationship	Existential restriction modifier (core metadata concept)	2
Hereditary sclerosing poikiloderma of Weary (disorder)	Associated morphology	Poikiloderma	false	Inferred relationship	Existential restriction modifier (core metadata concept)	2
Hereditary sclerosing poikiloderma of Weary (disorder)	Finding site	Microscopic skin vascular structure (body structure)	false	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Hereditary sclerosing poikiloderma of Weary (disorder)	Finding site	Skin structure	true	Inferred relationship	Existential restriction modifier (core metadata concept)	2
Hereditary sclerosing poikiloderma of Weary (disorder)	Associated morphology	Poikiloderma	true	Inferred relationship	Existential restriction modifier (core metadata concept)	2
Hereditary sclerosing poikiloderma of Weary (disorder)	Associated morphology	Telangiectasis	false	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Hereditary sclerosing poikiloderma of Weary (disorder)	Is a	Hereditary sclerosing poikiloderma	true	Inferred relationship	Existential restriction modifier (core metadata concept)

Inbound Relationships

Type

Active

Source

Characteristic

Refinability

Group

Reference Sets

GB English

US English

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Id	Description	Lang	Type	Status	Case?	Module
1771700010	Hereditary sclerosing poikiloderma of Weary (disorder)	en	Fully specified name	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
1782784011	Hereditary sclerosing poikiloderma of Weary	en	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
1771700010	Hereditary sclerosing poikiloderma of Weary (disorder)	en	Fully specified name	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
1782784011	Hereditary sclerosing poikiloderma of Weary	en	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
3450521001000117	Poikilodermie, hereditäre sklerosierende, Typ Weary	de	Synonym (core metadata concept)	Active	Entire term case sensitive (core metadata concept)	SNOMED CT Switzerland NRC maintained Module
6304331000241119	poïkilodermie sclérosante héréditaire de Weary	fr	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT Switzerland NRC maintained Module
6304331000241119	poïkilodermie sclérosante héréditaire de Weary	fr	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT Switzerland NRC maintained Module
3450521001000117	Poikilodermie, hereditäre sklerosierende, Typ Weary	de	Synonym (core metadata concept)	Active	Entire term case sensitive (core metadata concept)	SNOMED CT Switzerland NRC maintained Module