1260390003: dystonie door Lesch-Nyhan-syndroom (aandoening)

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

\Head finding (finding)\Finding of brain\Disorder of brain (disorder)\Extrapyramidal disease\Dystonia\Dystonia due to hereditary disease (disorder)\Dystonia due to Lesch Nyhan syndrome (disorder)
\Head finding (finding)\Disorder of head (disorder)\Disorder of brain (disorder)\Extrapyramidal disease\Dystonia\Dystonia due to hereditary disease (disorder)\Dystonia due to Lesch Nyhan syndrome (disorder)

\Finding of movement (finding)\Movement disorder\Extrapyramidal disease\Dystonia\Dystonia due to hereditary disease (disorder)\Dystonia due to Lesch Nyhan syndrome (disorder)

\Central nervous system finding\Finding of brain\Disorder of brain (disorder)\Extrapyramidal disease\Dystonia\Dystonia due to hereditary disease (disorder)\Dystonia due to Lesch Nyhan syndrome (disorder)
\Central nervous system finding\Disorder of the central nervous system (disorder)\Central nervous system complication\Dystonia due to hereditary disease (disorder)\Dystonia due to Lesch Nyhan syndrome (disorder)
\Central nervous system finding\Disorder of the central nervous system (disorder)\Disorder of brain (disorder)\Extrapyramidal disease\Dystonia\Dystonia due to hereditary disease (disorder)\Dystonia due to Lesch Nyhan syndrome (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 hereditary disease (disorder)\Dystonia due to Lesch Nyhan syndrome (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 hereditary disease (disorder)\Dystonia due to Lesch Nyhan syndrome (disorder)
\Disease\Disorder of head (disorder)\Disorder of brain (disorder)\Extrapyramidal disease\Dystonia\Dystonia due to hereditary disease (disorder)\Dystonia due to Lesch Nyhan syndrome (disorder)
\Disease\Movement disorder\Extrapyramidal disease\Dystonia\Dystonia due to hereditary disease (disorder)\Dystonia due to Lesch Nyhan syndrome (disorder)

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

Descriptions:

Expanded Value Set

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
Dystonia due to Lesch Nyhan syndrome (disorder)	Interprets	Movement	true	Inferred relationship	Some	3
Dystonia due to Lesch Nyhan syndrome (disorder)	Due to	Lesch-Nyhan syndrome	true	Inferred relationship	Some	2
Dystonia due to Lesch Nyhan syndrome (disorder)	Finding site	Extrapyramidal system structure	true	Inferred relationship	Some	1
Dystonia due to Lesch Nyhan syndrome (disorder)	Is a	Dystonia due to hereditary disease (disorder)	true	Inferred relationship	Some

Inbound Relationships

Type

Active

Source

Characteristic

Refinability

Group

This concept is not in any reference sets

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Id	Description	Lang	Type	Status	Case?	Module
5160302018	Dystonia due to Lesch Nyhan syndrome (disorder)	en	Fully specified name	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
5160704019	Dystonia due to Lesch Nyhan syndrome	en	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
14274801000146114	dystonie door syndroom van Lesch-Nyhan	nl	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT Netherlands NRC maintained module (core metadata concept)
14274811000146111	dystonie door Lesch-Nyhan-syndroom	nl	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT Netherlands NRC maintained module (core metadata concept)
14274821000146118	dystonie door complete HPRT-deficiëntie	nl	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT Netherlands NRC maintained module (core metadata concept)
14274831000146116	complete deficiëntie van hypoxanthine-guaninefosforibosyltransferase	nl	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT Netherlands NRC maintained module (core metadata concept)
14274841000146112	dystonie door Lesch-Nyhan-syndroom (aandoening)	nl	Fully specified name	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT Netherlands NRC maintained module (core metadata concept)