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32123005: Hooft's syndrome (disorder)


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

Descriptions:

Id Description Lang Type Status Case? Module
53673010 Hooft's syndrome en Synonym Active Entire term case sensitive SNOMED CT core module
53674016 Hypolipidemia syndrome en Synonym Active Entire term case insensitive SNOMED CT core module
53675015 Hypolipemia-tryptophan abnormality en Synonym Active Entire term case insensitive SNOMED CT core module
485141010 Hypolipaemia-tryptophan abnormality en Synonym Active Entire term case insensitive SNOMED CT core module
485142015 Hypolipidaemia syndrome en Synonym Active Entire term case insensitive SNOMED CT core module
763370012 Hooft's syndrome (disorder) en Fully specified name Active Entire term case sensitive SNOMED CT core module
2838257016 Hooft syndrome en Synonym Active Entire term case sensitive SNOMED CT core module


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Hooft's syndrome Is a Disorder of tryptophan metabolism true Inferred relationship Existential restriction modifier
Hooft's syndrome Occurrence Congenital false Inferred relationship Existential restriction modifier
Hooft's syndrome Finding site Body system structure false Inferred relationship Existential restriction modifier

Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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