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124346009: Deficiency of riboflavin mononucleotide adenylyltransferase (disorder)


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

Descriptions:

Id Description Lang Type Status Case? Module
204095014 Deficiency of FAD pyrophosphorylase en Synonym Active Initial character case insensitive SNOMED CT core
204096010 Deficiency of FMN adenylyltransferase en Synonym Active Initial character case insensitive SNOMED CT core
2913723015 Deficiency of riboflavin mononucleotide adenylyltransferase (disorder) en Fully specified name Active Case insensitive SNOMED CT core
2914157010 Deficiency of riboflavin mononucleotide adenylyltransferase en Synonym Active Case insensitive SNOMED CT core


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Deficiency of FMN adenylyltransferase Is a Deficiency of transferase true Inferred relationship Some
Deficiency of FMN adenylyltransferase 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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