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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


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Parkinsonism due to prion disease (disorder) est un(e) (attribut) Secondary parkinsonism true Inferred relationship Some
Parkinsonism due to prion disease (disorder) est un(e) (attribut) complication liée au système nerveux central true Inferred relationship Some
Parkinsonism due to prion disease (disorder) Due to maladie à prion true Inferred relationship Some 2
Parkinsonism due to prion disease (disorder) localisation d'une constatation (attribut) Basal ganglion structure (body structure) true Inferred relationship Some 1
Parkinsonism due to prion disease (disorder) interprète (attribut) Movement (observable entity) true Inferred relationship Some 3
Parkinsonism due to prion disease (disorder) a pour interprétation (attribut) lent true Inferred relationship Some 3

Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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