238834002: Hereditary sclerosing poikiloderma (disorder)

• SNOMED CT Concept\Clinical finding\...
• \Skin AND/OR mucosa finding\Skin finding\Disorder of skin\Degenerative skin disorder\Atrophic condition of skin\Poikiloderma\Hereditary sclerosing poikiloderma
• \General finding of soft tissue\Skin finding\Disorder of skin\Degenerative skin disorder\Atrophic condition of skin\Poikiloderma\Hereditary sclerosing poikiloderma
• \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\Poikiloderma\Hereditary sclerosing poikiloderma
• \Integumentary system finding\Disorder of integument\Hereditary disorder of the integument\Hereditary sclerosing poikiloderma
• \Integumentary system finding\Disorder of integument\Disorder of skin and/or subcutaneous tissue\Disorder of skin\Degenerative skin disorder\Atrophic condition of skin\Poikiloderma\Hereditary sclerosing poikiloderma
• \Integumentary system finding\Skin finding\Disorder of skin\Degenerative skin disorder\Atrophic condition of skin\Poikiloderma\Hereditary sclerosing poikiloderma
• \Disease\Genetic disease\Hereditary disease\Hereditary disorder by system\Hereditary disorder of the integument\Hereditary sclerosing poikiloderma
• \Disease\Degenerative disorder\Degenerative skin disorder\Atrophic condition of skin\Poikiloderma\Hereditary sclerosing poikiloderma
• \Disease\Disorder of body system\Hereditary disorder by system\Hereditary disorder of the integument\Hereditary sclerosing poikiloderma
• \Disease\Disorder of body system\Disorder of integument\Hereditary disorder of the integument\Hereditary sclerosing poikiloderma
• \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\Poikiloderma\Hereditary sclerosing poikiloderma
• \Disease\Disorder of soft tissue\Disorder of skin and/or subcutaneous tissue\Disorder of skin\Degenerative skin disorder\Atrophic condition of skin\Poikiloderma\Hereditary sclerosing poikiloderma

Status: current, Primitive. Date: 31-Jan 2002. Module: SNOMED CT core

Descriptions:

Id	Description	Lang	Type	Status	Case?	Module
357950017	Weary-Kindler syndrome	en	Synonym	Active	Case sensitive	SNOMED CT core
357951018	Hereditary sclerosing poikiloderma	en	Synonym	Active	Case insensitive	SNOMED CT core
627769014	Hereditary sclerosing poikiloderma (disorder)	en	Fully specified name	Active	Case insensitive	SNOMED CT core

Expanded Value Set

Reference Sets

Australian emergency department reference set

Clinical finding foundation reference set

Australian dialect reference set

Problem/Diagnosis reference set

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