1260399002: dystonie door ziekte van Hartnup (aandoening)

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

\Head finding (finding)\Finding of brain\Disorder of brain (disorder)\Extrapyramidal disease\Dystonia\Dystonia due to neutral 1 amino acid transport defect (disorder)
\Head finding (finding)\Disorder of head (disorder)\Disorder of brain (disorder)\Extrapyramidal disease\Dystonia\Dystonia due to neutral 1 amino acid transport defect (disorder)

\Finding of movement (finding)\Movement disorder\Extrapyramidal disease\Dystonia\Dystonia due to neutral 1 amino acid transport defect (disorder)

\Central nervous system finding\Finding of brain\Disorder of brain (disorder)\Extrapyramidal disease\Dystonia\Dystonia due to neutral 1 amino acid transport defect (disorder)
\Central nervous system finding\Disorder of the central nervous system (disorder)\Central nervous system complication\Dystonia due to neutral 1 amino acid transport defect (disorder)
\Central nervous system finding\Disorder of the central nervous system (disorder)\Disorder of brain (disorder)\Extrapyramidal disease\Dystonia\Dystonia due to neutral 1 amino acid transport defect (disorder)

\Disease\Disorder of body system\Disorder of nervous system (disorder)\Disorder of the central nervous system (disorder)\Central nervous system complication\Dystonia due to neutral 1 amino acid transport defect (disorder)
\Disease\Disorder of body system\Disorder of nervous system (disorder)\Disorder of the central nervous system (disorder)\Disorder of brain (disorder)\Extrapyramidal disease\Dystonia\Dystonia due to neutral 1 amino acid transport defect (disorder)
\Disease\Disorder of head (disorder)\Disorder of brain (disorder)\Extrapyramidal disease\Dystonia\Dystonia due to neutral 1 amino acid transport defect (disorder)
\Disease\Movement disorder\Extrapyramidal disease\Dystonia\Dystonia due to neutral 1 amino acid transport defect (disorder)

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

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 (core metadata concept) SNOMED CT core

5160321014 Dystonia due to Hartnup disease en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core

5160349019 Dystonia due to neutral 1 amino acid transport defect en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core

14275861000146114 dystonie door ziekte van Hartnup nl Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT Netherlands NRC maintained module (core metadata concept)

14275871000146115 dystonie door ziekte van Hartnup (aandoening) nl Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT Netherlands NRC maintained module (core metadata concept)

Expanded Value Set

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

Inbound Relationships

Type

Active

Source

Characteristic

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This concept is not in any reference sets