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725392005: Autosomal dominant striatal neurodegeneration (disorder)


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

Descriptions:

Id Description Lang Type Status Case? Module
5403452015 An adult-onset movement disorder characterized by bradykinesia, dysarthria and muscle rigidity. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
5403453013 An adult-onset movement disorder characterised by bradykinesia, dysarthria and muscle rigidity. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
3441978014 Autosomal dominant striatal neurodegeneration (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
3441979018 Autosomal dominant striatal neurodegeneration en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
3441980015 ADSD - autosomal dominant striatal neurodegeneration en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
886521000172114 ADSD - autosomal dominant striatal neurodegeneration fr Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
887481000172111 neurodégénérescence striatale autosomique dominante fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
3393911001000114 Neurodegeneration, striatale, autosomal-dominante 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
An adult-onset movement disorder characterized by bradykinesia, dysarthria and muscle rigidity. Is a Autosomal dominant hereditary disorder (disorder) true Inferred relationship Some
An adult-onset movement disorder characterized by bradykinesia, dysarthria and muscle rigidity. Is a Parkinsonism true Inferred relationship Some
An adult-onset movement disorder characterized by bradykinesia, dysarthria and muscle rigidity. Is a Hereditary disorder of nervous system false Inferred relationship Some
An adult-onset movement disorder characterized by bradykinesia, dysarthria and muscle rigidity. Is a Cerebral degeneration (disorder) true Inferred relationship Some
An adult-onset movement disorder characterized by bradykinesia, dysarthria and muscle rigidity. Associated morphology dégénérescence false Inferred relationship Some 1
An adult-onset movement disorder characterized by bradykinesia, dysarthria and muscle rigidity. Finding site Corpus striatum structure true Inferred relationship Some 1
An adult-onset movement disorder characterized by bradykinesia, dysarthria and muscle rigidity. Associated morphology Degenerative abnormality true Inferred relationship Some 1
An adult-onset movement disorder characterized by bradykinesia, dysarthria and muscle rigidity. Is a Hereditary degenerative disease of central nervous system true Inferred relationship Some
An adult-onset movement disorder characterized by bradykinesia, dysarthria and muscle rigidity. Interprets mouvement false Inferred relationship Some 3
An adult-onset movement disorder characterized by bradykinesia, dysarthria and muscle rigidity. Has interpretation Slow false Inferred relationship Some 3
An adult-onset movement disorder characterized by bradykinesia, dysarthria and muscle rigidity. Interprets Movement observable true Inferred relationship Some 2
An adult-onset movement disorder characterized by bradykinesia, dysarthria and muscle rigidity. Has interpretation Slow true Inferred relationship Some 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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