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124239003: Deficiency of guanidinoacetate methyltransferase (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
203821017 Deficiency of guanidinoacetate methyltransferase en Synonym Active Entire term case insensitive SNOMED CT core module
473085018 Guanidinoacetate methyltransferase deficiency en Synonym Active Entire term case insensitive SNOMED CT core module
727759016 Deficiency of guanidinoacetate methyltransferase (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 guanidinoacetate methyltransferase Is a Deficiency of transferase true Inferred relationship Existential restriction modifier
Deficiency of guanidinoacetate methyltransferase Is a Disorder of creatine synthesis true Inferred relationship Existential restriction modifier
Deficiency of guanidinoacetate methyltransferase Finding site Body system structure false Inferred relationship Existential restriction modifier
Deficiency of guanidinoacetate methyltransferase Occurrence Congenital true Inferred relationship Existential restriction modifier 1

Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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