402600008: Xeroderma in genetic syndrome (disorder)

• SNOMED CT Concept\Clinical finding\...
• \Skin AND/OR mucosa finding\Skin finding\...
• \Finding of moistness of skin\Xeroderma\Xeroderma in genetic syndrome
• \Disorder of skin\Xeroderma\Xeroderma in genetic syndrome
• \General finding of soft tissue\Skin finding\Finding of moistness of skin\Xeroderma\Xeroderma in genetic syndrome
• \General finding of soft tissue\Skin finding\Disorder of skin\Xeroderma\Xeroderma in genetic syndrome
• \General finding of soft tissue\Disorder of soft tissue\Disorder of skin and/or subcutaneous tissue\Disorder of skin\Xeroderma\Xeroderma in genetic syndrome
• \Integumentary system finding\Disorder of integument\Disorder of skin and/or subcutaneous tissue\Disorder of skin\Xeroderma\Xeroderma in genetic syndrome
• \Integumentary system finding\Skin finding\Finding of moistness of skin\Xeroderma\Xeroderma in genetic syndrome
• \Integumentary system finding\Skin finding\Disorder of skin\Xeroderma\Xeroderma in genetic syndrome
• \Disease\Disorder of body system\Disorder of integument\Disorder of skin and/or subcutaneous tissue\Disorder of skin\Xeroderma\Xeroderma in genetic syndrome
• \Disease\Disorder of soft tissue\Disorder of skin and/or subcutaneous tissue\Disorder of skin\Xeroderma\Xeroderma in genetic syndrome

Status: current, Primitive. Date: 31-Jul 2003. Module: SNOMED CT core

Descriptions:

Id	Description	Lang	Type	Status	Case?	Module
1770524011	Xeroderma in genetic syndrome (disorder)	en	Fully specified name	Active	Case insensitive	SNOMED CT core
1781717014	Xeroderma in genetic syndrome	en	Synonym	Active	Case insensitive	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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