238870004: Hutchinson-Gilford syndrome (disorder)

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

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

Descriptions:

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

Expanded Value Set

Reference Sets

Australian emergency department reference set

Clinical finding foundation reference set

Problem/Diagnosis reference set

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