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124910006: Deficiency of biotin (disorder)


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

Descriptions:

Id Description Lang Type Status Case? Module
193399016 Disorder of biotin en Synonym Active Case insensitive SNOMED CT core
2771686013 Deficiency of biotin en Synonym Active Case insensitive SNOMED CT core
728670015 Deficiency of biotin (disorder) en Fully specified name Active Case insensitive SNOMED CT core


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Disorder of biotin Is a Vitamin disease true Inferred relationship Some
Disorder of biotin Finding site Body system structure false Inferred relationship Some

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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