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783012006: Parkinsonian pyramidal syndrome (disorder)


Status: current, Not sufficiently defined by necessary conditions definition status. Date: 31-Jul 2019. Module: SNOMED CT core module

Descriptions:

Id Description Lang Type Status Case? Module
3757139016 Parkinsonian pyramidal syndrome (disorder) en Fully specified name Active Entire term case insensitive SNOMED CT core module
3757140019 Pallidopyramidal syndrome en Synonym Active Entire term case insensitive SNOMED CT core module
3757141015 Parkinsonian pyramidal syndrome 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
Parkinsonian pyramidal syndrome Is a Autosomal recessive hereditary disorder true Inferred relationship Existential restriction modifier
Parkinsonian pyramidal syndrome Is a Parkinsonism due to heredodegenerative disorder true Inferred relationship Existential restriction modifier
Parkinsonian pyramidal syndrome Is a Hereditary disorder of nervous system true Inferred relationship Existential restriction modifier
Parkinsonian pyramidal syndrome Finding site Basal ganglion structure true Inferred relationship Existential restriction modifier 1
Parkinsonian pyramidal syndrome Due to Hereditary degenerative disease of central nervous system true Inferred relationship Existential restriction modifier 2
Parkinsonian pyramidal syndrome Interprets Movement true Inferred relationship Existential restriction modifier 4
Parkinsonian pyramidal syndrome Has interpretation Slow true Inferred relationship Existential restriction modifier 4

Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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