FHIR © HL7.org  |  Server Home  |  FHIR Server FHIR Server 3.7.13  |  FHIR Version n/a  User: [n/a]

716662004: Autosomal dominant late onset Parkinson disease (disorder)


Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jul 2016. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
3307125015 Autosomal dominant late onset Parkinson disease (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
3307126019 Autosomal dominant late onset Parkinson disease en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
3307127011 Hereditary late onset Parkinson disease en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
3307128018 A form of Parkinson disease with age of onset of more than 50 years, tremor at rest, gait complaints and falls, bradykinesia, rigidity and painful cramps. Patients usually present a low risk of developing non-motor symptoms, dystonia, dyskinesia and levodopa-induced dyskinesia. The exact etiology is still unknown but mutations in the genes SNCA (4q21.3-q22), LRRK2 (12q12), and VPS35 (16q12) have been implicated in its pathogenesis. Transmission is autosomal dominant. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
3307129014 A form of Parkinson disease with age of onset of more than 50 years, tremor at rest, gait complaints and falls, bradykinesia, rigidity and painful cramps. Patients usually present a low risk of developing non-motor symptoms, dystonia, dyskinesia and levodopa-induced dyskinesia. The exact aetiology is still unknown but mutations in the genes SNCA (4q21.3-q22), LRRK2 (12q12), and VPS35 (16q12) have been implicated in its pathogenesis. Transmission is autosomal dominant. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Autosomal dominant late onset Parkinson disease (disorder) morphologie associée (attribut) Degenerative abnormality true Inferred relationship Some 1
Autosomal dominant late onset Parkinson disease (disorder) est un(e) (attribut) Hereditary degenerative disease of central nervous system true Inferred relationship Some
Autosomal dominant late onset Parkinson disease (disorder) Causative agent alpha-synucléine false Inferred relationship Some 1
Autosomal dominant late onset Parkinson disease (disorder) interprète (attribut) Movement (observable entity) true Inferred relationship Some 3
Autosomal dominant late onset Parkinson disease (disorder) a pour interprétation (attribut) lent true Inferred relationship Some 3
Autosomal dominant late onset Parkinson disease (disorder) est un(e) (attribut) Autosomal dominant hereditary disorder true Inferred relationship Some
Autosomal dominant late onset Parkinson disease (disorder) est un(e) (attribut) maladie de Parkinson (trouble) true Inferred relationship Some
Autosomal dominant late onset Parkinson disease (disorder) est un(e) (attribut) Hereditary disorder of nervous system false Inferred relationship Some
Autosomal dominant late onset Parkinson disease (disorder) localisation d'une constatation (attribut) Basal ganglion structure (body structure) true Inferred relationship Some 1

Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

Back to Start