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699038001: Hemoglobin variant screening requested (situation)


Status: current, Defined. Date: 31-Jan 2014. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
2982450013 Hemoglobin variant screening requested (situation) en Fully specified name Active Case insensitive SNOMED CT core
2982553012 Hemoglobin variant screening requested en Synonym Active Case insensitive SNOMED CT core
2989193017 Haemoglobin variant screening requested en Synonym Active Case insensitive SNOMED CT core


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Haemoglobin variant screening requested Is a Haematology test requested true Inferred relationship Some
Haemoglobin variant screening requested Associated procedure Haemoglobin variant test true Inferred relationship Some 1
Haemoglobin variant screening requested Subject relationship context Subject of record true Inferred relationship Some 1
Haemoglobin variant screening requested Temporal context Current or specified true Inferred relationship Some 1
Haemoglobin variant screening requested Procedure context Requested true Inferred relationship Some 1

Inbound Relationships Type Active Source Characteristic Refinability Group

Reference Sets

Situation with explicit context foundation reference set

Problem/Diagnosis reference set

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