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717942003: Brain dopamine-serotonin vesicular transport disease (disorder)


Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2017. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
3324411010 Brain dopamine-serotonin vesicular transport disease (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
3324412015 Brain dopamine-serotonin vesicular transport disease en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
5401644016 A rare infantile onset neurometabolic disease characterized by dystonia, parkinsonism, nonambulation, autonomic dysfunction, developmental delay and mood disturbances. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
5401645015 A rare infantile onset neurometabolic disease characterised by dystonia, parkinsonism, nonambulation, autonomic dysfunction, developmental delay and mood disturbances. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
3324411010 Brain dopamine-serotonin vesicular transport disease (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
3324411010 Brain dopamine-serotonin vesicular transport disease (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
3324412015 Brain dopamine-serotonin vesicular transport disease en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
3324412015 Brain dopamine-serotonin vesicular transport disease en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
3324413013 An infantile-onset neurometabolic disease with characteristics of dystonia, parkinsonism, nonambulation, autonomic dysfunction, developmental delay and mood disturbances. The prevalence is unknown. It has been described in 8 patients from one Saudi Arabian family to date. Caused by a mutation in the SLC18A2 gene (10q25), encoding the vesicular monoamine transporter 2 (VMAT2) which is responsible for the transport of dopamine and serotonin into synaptic vesicles. Mutations in this gene lead to the impairment of VMAT2 and consequently to problems with motor control, autonomic functioning and mood regulation. It is inherited in an autosomal recessive manner. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
5401644016 A rare infantile onset neurometabolic disease characterized by dystonia, parkinsonism, nonambulation, autonomic dysfunction, developmental delay and mood disturbances. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
5401645015 A rare infantile onset neurometabolic disease characterised by dystonia, parkinsonism, nonambulation, autonomic dysfunction, developmental delay and mood disturbances. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
3422291001000118 Störung des zerebralen vesikulären Dopamin-Serotonin-Transportes de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
999811000172115 déficit du transport vésiculaire cérébral de la dopamine et de la sérotonine fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
999811000172115 déficit du transport vésiculaire cérébral de la dopamine et de la sérotonine fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
3422291001000118 Störung des zerebralen vesikulären Dopamin-Serotonin-Transportes de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Brain dopamine-serotonin vesicular transport disease (disorder) Is a Dystonia true Inferred relationship Existential restriction modifier (core metadata concept)
Brain dopamine-serotonin vesicular transport disease (disorder) Is a Autosomal recessive hereditary disorder true Inferred relationship Existential restriction modifier (core metadata concept)
Brain dopamine-serotonin vesicular transport disease (disorder) Is a Metabolic disorder of transport (disorder) true Inferred relationship Existential restriction modifier (core metadata concept)
Brain dopamine-serotonin vesicular transport disease (disorder) Is a Hereditary disorder of nervous system (disorder) true Inferred relationship Existential restriction modifier (core metadata concept)
Brain dopamine-serotonin vesicular transport disease (disorder) Finding site Extrapyramidal system structure true Inferred relationship Existential restriction modifier (core metadata concept) 1
Brain dopamine-serotonin vesicular transport disease (disorder) Interprets Movement true Inferred relationship Existential restriction modifier (core metadata concept) 2

Inbound Relationships Type Active Source Characteristic Refinability Group

Reference Sets

Component annotation with string value reference set (foundation metadata concept)

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