238834002: Hereditary sclerosing poikiloderma (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

\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
\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

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

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

Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2002. Module: SNOMED CT core

Descriptions:

Expanded Value Set

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
Hereditary sclerosing poikiloderma	Is a	Hereditary disorder of the integument (disorder)	true	Inferred relationship	Existential restriction modifier (core metadata concept)
Hereditary sclerosing poikiloderma	Is a	Disorder of skin (disorder)	false	Inferred relationship	Existential restriction modifier (core metadata concept)
Hereditary sclerosing poikiloderma	Finding site	Skin structure	false	Inferred relationship	Existential restriction modifier (core metadata concept)
Hereditary sclerosing poikiloderma	Associated morphology	Poikiloderma	true	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Hereditary sclerosing poikiloderma	Finding site	Skin structure	true	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Hereditary sclerosing poikiloderma	Is a	Poikiloderma (disorder)	true	Inferred relationship	Existential restriction modifier (core metadata concept)

Inbound Relationships	Type	Active	Source	Characteristic	Refinability	Group
Hereditary acrokeratotic poikiloderma of Weary	Is a	True	Hereditary sclerosing poikiloderma	Inferred relationship	Existential restriction modifier (core metadata concept)
Kindler epidermolysis bullosa	Is a	True	Hereditary sclerosing poikiloderma	Inferred relationship	Existential restriction modifier (core metadata concept)
Hereditary fibrosing poikiloderma, tendon contractures, myopathy, pulmonary fibrosis syndrome (disorder)	Is a	True	Hereditary sclerosing poikiloderma	Inferred relationship	Existential restriction modifier (core metadata concept)
Hereditary sclerosing poikiloderma of Weary (disorder)	Is a	True	Hereditary sclerosing poikiloderma	Inferred relationship	Existential restriction modifier (core metadata concept)

Reference Sets

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US English

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Id	Description	Lang	Type	Status	Case?	Module
357950017	Weary-Kindler syndrome	en	Synonym (core metadata concept)	Active	Entire term case sensitive (core metadata concept)	SNOMED CT core
357951018	Hereditary sclerosing poikiloderma	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
627769014	Hereditary sclerosing poikiloderma (disorder)	en	Fully specified name	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
357950017	Weary-Kindler syndrome	en	Synonym (core metadata concept)	Active	Entire term case sensitive (core metadata concept)	SNOMED CT core
357951018	Hereditary sclerosing poikiloderma	en	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
357951018	Hereditary sclerosing poikiloderma	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
627769014	Hereditary sclerosing poikiloderma (disorder)	en	Fully specified name	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
627769014	Hereditary sclerosing poikiloderma (disorder)	en	Fully specified name	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
6312201000241112	poïkilodermie sclérosante héréditaire	fr	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT Switzerland NRC maintained Module
6312201000241112	poïkilodermie sclérosante héréditaire	fr	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT Switzerland NRC maintained Module