297226004: Disorder of creatine synthesis (disorder)

SNOMED CT Concept\Clinical finding (finding)\Disease\...

\Genetic disease\Hereditary disease\Hereditary metabolic disease\Inborn error of metabolism\Disorder of creatine synthesis

\Disorder of foetus and/or newborn\Congenital disease\Inborn error of metabolism\Disorder of creatine synthesis

\Metabolic disease\Hereditary metabolic disease\Inborn error of metabolism\Disorder of creatine synthesis
\Metabolic disease\Disorder of organic acid metabolism (disorder)\Disorder of amino acid metabolism (disorder)\Disorder of creatine synthesis

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

Descriptions:

Id Description Lang Type Status Case? Module

437708018 Disorder of creatine synthesis en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core

692534012 Disorder of creatine synthesis (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core

437708018 Disorder of creatine synthesis en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core

437708018 Disorder of creatine synthesis en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core

692534012 Disorder of creatine synthesis (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core

692534012 Disorder of creatine synthesis (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core

5164661000241111 trouble du métabolisme de la créatine fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module

5164661000241111 trouble du métabolisme de la créatine fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module

Expanded Value Set

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
Disorder of creatine synthesis	Is a	Disorder of amino acid metabolism (disorder)	true	Inferred relationship	Existential restriction modifier (core metadata concept)
Disorder of creatine synthesis	Finding site	Body system structure	false	Inferred relationship	Existential restriction modifier (core metadata concept)
Disorder of creatine synthesis	Occurrence	Congenital	true	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Disorder of creatine synthesis	Is a	Inborn error of metabolism	true	Inferred relationship	Existential restriction modifier (core metadata concept)

Inbound Relationships	Type	Active	Source	Characteristic	Refinability	Group
Deficiency of guanidinoacetate methyltransferase	Is a	True	Disorder of creatine synthesis	Inferred relationship	Existential restriction modifier (core metadata concept)
Arginine:glycine amidinotransferase deficiency	Is a	True	Disorder of creatine synthesis	Inferred relationship	Existential restriction modifier (core metadata concept)

This concept is not in any reference sets