74320008: Woolf's syndrome (disorder)

• SNOMED CT Concept\Clinical finding (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 (disorder)\Albinism\Woolf's syndrome
• \Disorder of foetus and/or newborn\Congenital disease (disorder)\...
• \Congenital malformation\Albinism\Woolf's syndrome
• \Inborn error of metabolism\Albinism\Woolf's syndrome
• \Metabolic disease\Hereditary metabolic disease\Inborn error of metabolism\Albinism\Woolf's syndrome
• \Metabolic disease\Disorder of organic acid metabolism\Disorder of amino acid metabolism\Disorder of amino acid and organic acid metabolism\Disorder of tyrosine metabolism\Woolf's syndrome
• \Developmental disorder\Developmental hereditary disorder\Albinism\Woolf's syndrome
• \Developmental disorder\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
814806017	Woolf's syndrome (disorder)	en	Fully specified name	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

Expanded Value Set

This concept is not in any reference sets

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