297232009: 3-Methylglutaconic aciduria type 3 (disorder)

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

\Genetic disease\Hereditary disease\Autosomal hereditary disorder\Autosomal recessive hereditary disorder\3-Methylglutaconic aciduria type 3

\Metabolic disease\Disorder of organic acid metabolism\Disorder of amino acid metabolism\Disorder of amino acid and organic acid metabolism\Disorder of branched-chain amino acid metabolism\3-Methylglutaconic aciduria\3-Methylglutaconic aciduria type 3

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

437715014 Costeff syndrome en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core

437716010 3-Methylglutaconic aciduria type 3 en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core

692541018 3-Methylglutaconic aciduria type 3 (disorder) en Fully specified name Active Entire term case sensitive (core metadata concept) SNOMED CT core

Expanded Value Set

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
3-Methylglutaconic aciduria type 3	Is a	3-Methylglutaconic aciduria	true	Inferred relationship	Some
3-Methylglutaconic aciduria type 3	Occurrence	Congenital	false	Inferred relationship	Some
3-Methylglutaconic aciduria type 3	Finding site	Body system structure	false	Inferred relationship	Some
3-Methylglutaconic aciduria type 3	Is a	Autosomal recessive hereditary disorder	true	Inferred relationship	Some

Inbound Relationships

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This concept is not in any reference sets