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1176989007: Parkinsonism due to prion disease (disorder)


Status: current, Sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Oct 2021. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
4643049019 Parkinsonism due to prion disease (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
4643050019 Parkinsonism due to prion disease en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
4643049019 Parkinsonism due to prion disease (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
4643050019 Parkinsonism due to prion disease en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
6447071000241113 parkinsonisme dû à une maladie à prions fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
6447081000241110 syndrome parkinsonien dû à une maladie à prions fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
6447071000241113 parkinsonisme dû à une maladie à prions fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
6447081000241110 syndrome parkinsonien dû à une maladie à prions fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Parkinsonism due to prion disease (disorder) Is a Secondary parkinsonism true Inferred relationship Existential restriction modifier (core metadata concept)
Parkinsonism due to prion disease (disorder) Is a Central nervous system complication true Inferred relationship Existential restriction modifier (core metadata concept)
Parkinsonism due to prion disease (disorder) Due to Prion disease true Inferred relationship Existential restriction modifier (core metadata concept) 2
Parkinsonism due to prion disease (disorder) Finding site Basal ganglion structure (body structure) true Inferred relationship Existential restriction modifier (core metadata concept) 1
Parkinsonism due to prion disease (disorder) Interprets Movement true Inferred relationship Existential restriction modifier (core metadata concept) 3
Parkinsonism due to prion disease (disorder) Has interpretation Slow true Inferred relationship Existential restriction modifier (core metadata concept) 3

Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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