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15758261000119106: Presence of unidentified hemoglobin variant (finding)


Status: current, Primitive. Date: 31-Jan 2017. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
3330540011 Presence of unidentified hemoglobin variant (finding) en Fully specified name Active Case insensitive SNOMED CT core
3331350015 Presence of unidentified hemoglobin variant en Synonym Active Case insensitive SNOMED CT core
3331351016 Presence of unidentified haemoglobin variant en Synonym Active Case insensitive SNOMED CT core


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Presence of unidentified haemoglobin variant Is a Abnormal finding on evaluation procedure true Inferred relationship Some
Presence of unidentified haemoglobin variant Is a Haemoglobin variant finding true Inferred relationship Some
Presence of unidentified haemoglobin variant Interprets Haemoglobin variant test true Inferred relationship Some 1
Presence of unidentified haemoglobin variant Has interpretation Abnormal true Inferred relationship Some 1
Presence of unidentified haemoglobin variant Is a Abnormal presence of haemoglobin false Inferred relationship Some
Presence of unidentified haemoglobin variant Has interpretation Abnormal presence of false Inferred relationship Some 1
Presence of unidentified haemoglobin variant Interprets Detection of haemoglobin false Inferred relationship Some 1

Inbound Relationships Type Active Source Characteristic Refinability Group

Reference Sets

Australian emergency department reference set

Queensland allied health clinical finding reference set

Clinical finding foundation reference set

Problem/Diagnosis reference set

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