74320008: Woolf's syndrome (disorder)

• SNOMED CT Concept\constatation clinique\Disease\...
• \Genetic disease\maladie héréditaire\...
• \Developmental hereditary disorder\Albinism\Woolf's syndrome
• \Inborn error of metabolism\Albinism\Woolf's syndrome
• \trouble de la pigmentation\Albinism\Woolf's syndrome
• \trouble métabolique\Disorder of organic acid metabolism\Disorder of amino acid metabolism\Disorder of amino acid and organic acid metabolism\Disorder of tyrosine metabolism (disorder)\Woolf's syndrome
• \trouble métabolique\Inborn error of metabolism\Albinism\Woolf's syndrome
• \Congenital disease\Congenital malformation\Albinism\Woolf's syndrome
• \Congenital disease\Inborn error of metabolism\Albinism\Woolf's syndrome
• \trouble du développement\Developmental hereditary disorder\Albinism\Woolf's syndrome
• \trouble du développement\Congenital malformation\Albinism\Woolf's syndrome

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

Descriptions:

Id	Description	Lang	Type	Status	Case?	Module
123422011	Woolf's syndrome	en	Synonym (core metadata concept)	Active	Entire term case sensitive (core metadata concept)	SNOMED CT core
2839481017	Woolf syndrome	en	Synonym (core metadata concept)	Active	Entire term case sensitive (core metadata concept)	SNOMED CT core
814806017	Woolf's syndrome (disorder)	en	Fully specified name	Active	Entire term case sensitive (core metadata concept)	SNOMED CT core

Expanded Value Set

This concept is not in any reference sets

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