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124213001: Deficiency of unspecific monooxygenase (disorder)


Status: current, Not sufficiently defined by necessary conditions definition status. Date: 31-Jan 2002. Module: SNOMED CT core module

Descriptions:

Id Description Lang Type Status Case? Module
203771013 Deficiency of microsomal monooxygenase en Synonym Active Entire term case insensitive SNOMED CT core module
203772018 Deficiency of microsomal P450 flavoprotein-linked monooxygenase en Synonym Active Only initial character case insensitive SNOMED CT core module
203773011 Deficiency of aryl-4-monooxygenase en Synonym Active Entire term case insensitive SNOMED CT core module
203774017 Deficiency of aryl hydrocarbon hydroxylase en Synonym Active Entire term case insensitive SNOMED CT core module
203775016 Deficiency of unspecific monooxygenase en Synonym Active Entire term case insensitive SNOMED CT core module
727717017 Deficiency of unspecific monooxygenase (disorder) en Fully specified name Active Entire term case insensitive SNOMED CT core module


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 Existential restriction modifier
Deficiency of unspecific monooxygenase Finding site Body system structure false Inferred relationship Existential restriction modifier

Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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