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124215008: Deficiency of phenylalanine 4-monooxygenase (disorder)


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

Descriptions:

Id Description Lang Type Status Case? Module
203784016 Deficiency of phenylalanine 4-hydroxylase en Synonym Active Case insensitive SNOMED CT core
203785015 Deficiency of phenylalaninase en Synonym Active Case insensitive SNOMED CT core
203786019 Deficiency of phenylalanine 4-monooxygenase en Synonym Active Case insensitive SNOMED CT core
727719019 Deficiency of phenylalanine 4-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 phenylalanine 4-monooxygenase Is a Specific enzyme deficiency true Inferred relationship Some
Deficiency of phenylalanine 4-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

Problem/Diagnosis reference set

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