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783012006: Parkinsonian pyramidal syndrome (disorder)


Status: current, Primitive. Date: 31-Jul 2019. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
3757139016 Parkinsonian pyramidal syndrome (disorder) en Fully specified name Active Case insensitive SNOMED CT core
3757140019 Pallidopyramidal syndrome en Synonym Active Case insensitive SNOMED CT core
3757141015 Parkinsonian pyramidal syndrome en Synonym Active Case insensitive SNOMED CT core
3757142010 A rare genetic neurological disorder with characteristics of the association of both parkinsonian (such as bradykinesia, rigidity and/or rest tremor) and pyramidal (such as increased reflexes, extensor plantar reflexes, pyramidal weakness or spasticity) manifestations, which vary according to the underlying associated disease (for example neurodegenerative disease, inborn errors of metabolism). en Definition Active Case sensitive SNOMED CT core


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Parkinsonian pyramidal syndrome Is a Autosomal recessive hereditary disorder true Inferred relationship Some
Parkinsonian pyramidal syndrome Is a Parkinsonism due to heredodegenerative disorder true Inferred relationship Some
Parkinsonian pyramidal syndrome Is a Hereditary disorder of nervous system true Inferred relationship Some
Parkinsonian pyramidal syndrome Finding site Basal ganglion structure true Inferred relationship Some 1
Parkinsonian pyramidal syndrome Due to Hereditary degenerative disease of central nervous system true Inferred relationship Some 2
Parkinsonian pyramidal syndrome Interprets Movement true Inferred relationship Some 4
Parkinsonian pyramidal syndrome Has interpretation Slow true Inferred relationship Some 4

Inbound Relationships Type Active Source Characteristic Refinability Group

Reference Sets

Australian emergency department reference set

Clinical finding foundation reference set

Problem/Diagnosis reference set

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