74320008: Woolf's syndrome (disorder)

• SNOMED CT Concept\Clinical finding\Disease\...
• \Genetic disease\Hereditary disease\...
• \Hereditary metabolic disease\Inborn error of metabolism\Albinism\Woolf's syndrome
• \Developmental hereditary disorder\Albinism\Woolf's syndrome
• \Disorder of pigmentation\Albinism\Woolf's syndrome
• \Metabolic disease\Hereditary metabolic disease\Inborn error of metabolism\Albinism\Woolf's syndrome
• \Metabolic disease\Organic acid metabolism disorder\Disorder of amino acid metabolism\Disorder of amino acid and organic acid metabolism\Disorder of tyrosine metabolism\Woolf's syndrome
• \Congenital disease\Congenital anomaly\Albinism\Woolf's syndrome
• \Congenital disease\Inborn error of metabolism\Albinism\Woolf's syndrome
• \Developmental disorder\Developmental hereditary disorder\Albinism\Woolf's syndrome
• \Developmental disorder\Congenital anomaly\Albinism\Woolf's syndrome

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

Descriptions:

Id	Description	Lang	Type	Status	Case?	Module
123422011	Woolf's syndrome	en	Synonym	Active	Case sensitive	SNOMED CT core
2839481017	Woolf syndrome	en	Synonym	Active	Case sensitive	SNOMED CT core
814806017	Woolf's 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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