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49607006: Biotin deficiency disease (disorder)


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

Descriptions:

Id Description Lang Type Status Case? Module
787304010 Biotin deficiency disease (disorder) en Fully specified name Active Case insensitive SNOMED CT core
82625017 Biotin deficiency disease en Synonym Active Case insensitive SNOMED CT core


0 descendants.

Expanded Value Set


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

Inbound Relationships Type Active Source Characteristic Refinability Group
Dermatosis associated with biotin deficiency Is a False Biotin deficiency disease Inferred relationship Some

Reference Sets

Australian emergency department reference set

Clinical finding foundation reference set

Australian dialect reference set

Problem/Diagnosis reference set

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