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18789002: Tryptophanuria (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
31681014 Tryptophanuria en Synonym Active Entire term case insensitive SNOMED CT core module
746347017 Tryptophanuria (disorder) en Fully specified name Active Entire term case insensitive SNOMED CT core module


1 descendants. Search Descendants:

Expanded Value Set


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

Inbound Relationships Type Active Source Characteristic Refinability Group
Tryptophanuria with dwarfism Is a True Tryptophanuria Inferred relationship Existential restriction modifier

This concept is not in any reference sets

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