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124213001: Deficiency of unspecific monooxygenase (disorder)


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

Descriptions:

Id Description Lang Type Status Case? Module
203771013 Deficiency of microsomal monooxygenase en Synonym Active Case insensitive SNOMED CT core
203772018 Deficiency of microsomal P450 flavoprotein-linked monooxygenase en Synonym Active Initial character case insensitive SNOMED CT core
203773011 Deficiency of aryl-4-monooxygenase en Synonym Active Case insensitive SNOMED CT core
203774017 Deficiency of aryl hydrocarbon hydroxylase en Synonym Active Case insensitive SNOMED CT core
203775016 Deficiency of unspecific monooxygenase en Synonym Active Case insensitive SNOMED CT core
727717017 Deficiency of unspecific monooxygenase (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
Deficiency of unspecific monooxygenase Is a Specific enzyme deficiency true Inferred relationship Some
Deficiency of unspecific monooxygenase 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

Australian dialect reference set

Problem/Diagnosis reference set

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