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1260399002: Dystonia due to neutral 1 amino acid transport defect (disorder)


Status: current, Sufficiently defined by necessary conditions definition status. Date: 31-Jan 2023. Module: SNOMED CT core module

Descriptions:

Id Description Lang Type Status Case? Module
5160320010 Dystonia due to neutral 1 amino acid transport defect (disorder) en Fully specified name Active Entire term case insensitive SNOMED CT core module
5160321014 Dystonia due to Hartnup disease en Synonym Active Only initial character case insensitive SNOMED CT core module
5160349019 Dystonia due to neutral 1 amino acid transport defect en Synonym Active Entire term case insensitive SNOMED CT core module


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Dystonia due to neutral 1 amino acid transport defect Is a Dystonia true Inferred relationship Existential restriction modifier
Dystonia due to neutral 1 amino acid transport defect Is a Central nervous system complication true Inferred relationship Existential restriction modifier
Dystonia due to neutral 1 amino acid transport defect Interprets Movement true Inferred relationship Existential restriction modifier 2
Dystonia due to neutral 1 amino acid transport defect Due to Neutral 1 amino acid transport defect true Inferred relationship Existential restriction modifier 3
Dystonia due to neutral 1 amino acid transport defect Finding site Extrapyramidal system structure 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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