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297233004: 3-Methylglutaconic aciduria type 4 (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
437717018 3-Methylglutaconic aciduria type 4 en Synonym Active Entire term case sensitive SNOMED CT core module
692543015 3-Methylglutaconic aciduria type 4 (disorder) en Fully specified name Active Entire term case sensitive SNOMED CT core module


1 descendants. Search Descendants:

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
3-Methylglutaconic aciduria type 4 Is a 3-Methylglutaconic aciduria true Inferred relationship Existential restriction modifier
3-Methylglutaconic aciduria type 4 Occurrence Congenital false Inferred relationship Existential restriction modifier
3-Methylglutaconic aciduria type 4 Finding site Body system structure false Inferred relationship Existential restriction modifier
3-Methylglutaconic aciduria type 4 Is a Autosomal recessive hereditary disorder true Inferred relationship Existential restriction modifier

Inbound Relationships Type Active Source Characteristic Refinability Group
3-methylglutaconic aciduria type IV with sensorineural deafness, encephalopathy and Leigh-like syndrome Is a True 3-Methylglutaconic aciduria type 4 Inferred relationship Existential restriction modifier

This concept is not in any reference sets

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