238870004: Hutchinson-Gilford syndrome (disorder)

• SNOMED CT Concept\Clinical finding\...
• \Skin AND/OR mucosa finding\Skin finding\Disorder of skin\Premature aging syndrome\Laminopathy with premature aging\Hutchinson-Gilford syndrome
• \General finding of soft tissue\Skin finding\Disorder of skin\Premature aging syndrome\Laminopathy with premature aging\Hutchinson-Gilford syndrome
• \General finding of soft tissue\Disorder of soft tissue\Disorder of skin and/or subcutaneous tissue\Disorder of skin\Premature aging syndrome\Laminopathy with premature aging\Hutchinson-Gilford syndrome
• \Integumentary system finding\Disorder of integument\Hereditary disorder of the integument\Premature aging syndrome\Laminopathy with premature aging\Hutchinson-Gilford syndrome
• \Integumentary system finding\Disorder of integument\Disorder of skin and/or subcutaneous tissue\Disorder of skin\Premature aging syndrome\Laminopathy with premature aging\Hutchinson-Gilford syndrome
• \Integumentary system finding\Skin finding\Disorder of skin\Premature aging syndrome\Laminopathy with premature aging\Hutchinson-Gilford syndrome
• \Disease\Genetic disease\Hereditary disease\Hereditary metabolic disease\Inborn error of metabolism\Premature aging syndrome\Laminopathy with premature aging\Hutchinson-Gilford syndrome
• \Disease\Genetic disease\Hereditary disease\Hereditary disorder by system\Hereditary disorder of the integument\Premature aging syndrome\Laminopathy with premature aging\Hutchinson-Gilford syndrome
• \Disease\Disorder of body system\Hereditary disorder by system\Hereditary disorder of the integument\Premature aging syndrome\Laminopathy with premature aging\Hutchinson-Gilford syndrome
• \Disease\Disorder of body system\Disorder of integument\Hereditary disorder of the integument\Premature aging syndrome\Laminopathy with premature aging\Hutchinson-Gilford syndrome
• \Disease\Disorder of body system\Disorder of integument\Disorder of skin and/or subcutaneous tissue\Disorder of skin\Premature aging syndrome\Laminopathy with premature aging\Hutchinson-Gilford syndrome
• \Disease\Metabolic disease\Hereditary metabolic disease\Inborn error of metabolism\Premature aging syndrome\Laminopathy with premature aging\Hutchinson-Gilford syndrome
• \Disease\Congenital disease\Inborn error of metabolism\Premature aging syndrome\Laminopathy with premature aging\Hutchinson-Gilford syndrome
• \Disease\Disorder of soft tissue\Disorder of skin and/or subcutaneous tissue\Disorder of skin\Premature aging syndrome\Laminopathy with premature aging\Hutchinson-Gilford syndrome

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

Descriptions:

Id	Description	Lang	Type	Status	Case?	Module
357996013	Hutchinson-Gilford syndrome	en	Synonym	Active	Entire term case sensitive	SNOMED CT core module
357997016	Progeria syndrome	en	Synonym	Active	Entire term case insensitive	SNOMED CT core module
357998014	Premature senility syndrome	en	Synonym	Active	Entire term case insensitive	SNOMED CT core module
627809017	Hutchinson-Gilford syndrome (disorder)	en	Fully specified name	Active	Entire term case sensitive	SNOMED CT core module
1784924019	Progeria	en	Synonym	Active	Entire term case insensitive	SNOMED CT core module

Expanded Value Set

This concept is not in any reference sets

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