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59531002: Tryptophan malabsorption syndrome (disorder)


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

Descriptions:

Id Description Lang Type Status Case? Module
798384012 Tryptophan malabsorption syndrome (disorder) en Fully specified name Active Case insensitive SNOMED CT core
98878014 Tryptophan malabsorption syndrome en Synonym Active Case insensitive SNOMED CT core
98879018 Blue diaper syndrome en Synonym Active Case insensitive SNOMED CT core


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Tryptophan malabsorption syndrome Is a Disorder of tryptophan metabolism true Inferred relationship Some
Tryptophan malabsorption syndrome Is a Congenital anomaly of trunk false Inferred relationship Some
Tryptophan malabsorption syndrome Is a Microscopic nephrocalcinosis true Inferred relationship Some
Tryptophan malabsorption syndrome Is a Hereditary disorder of the urinary system false Inferred relationship Some
Tryptophan malabsorption syndrome Associated morphology Pathologic calcification false Inferred relationship Some 1
Tryptophan malabsorption syndrome Associated morphology Pathologic calcification true Inferred relationship Some 1
Tryptophan malabsorption syndrome Finding site Kidney structure true Inferred relationship Some 1
Tryptophan malabsorption syndrome Occurrence Congenital false Inferred relationship Some
Tryptophan malabsorption syndrome Finding site Kidney structure false Inferred relationship Some 1

Inbound Relationships Type Active Source Characteristic Refinability Group

Reference Sets

Australian emergency department reference set

Clinical finding foundation reference set

Problem/Diagnosis reference set

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