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1176989007: Parkinsonism due to prion disease (disorder)


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

Descriptions:

Id Description Lang Type Status Case? Module
4643049019 Parkinsonism due to prion disease (disorder) en Fully specified name Active Entire term case insensitive SNOMED CT core module
4643050019 Parkinsonism due to prion disease en Synonym Active Entire term case insensitive SNOMED CT core module


0 descendants.

Expanded Value Set


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

Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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