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716662004: Autosomal dominant late onset Parkinson disease (disorder)


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

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 SNOMED CT core module
3307126019 Autosomal dominant late onset Parkinson disease en Synonym Active Only initial character case insensitive SNOMED CT core module
3307127011 Hereditary late onset Parkinson disease en Synonym Active Only initial character case insensitive SNOMED CT core module


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Autosomal dominant late onset Parkinson disease Is a Autosomal dominant hereditary disorder true Inferred relationship Existential restriction modifier
Autosomal dominant late onset Parkinson disease Is a Parkinson's disease true Inferred relationship Existential restriction modifier
Autosomal dominant late onset Parkinson disease Is a Hereditary disorder of nervous system false Inferred relationship Existential restriction modifier
Autosomal dominant late onset Parkinson disease Finding site Basal ganglion structure true Inferred relationship Existential restriction modifier 1
Autosomal dominant late onset Parkinson disease Associated morphology Degenerative abnormality true Inferred relationship Existential restriction modifier 1
Autosomal dominant late onset Parkinson disease Is a Hereditary degenerative disease of central nervous system true Inferred relationship Existential restriction modifier
Autosomal dominant late onset Parkinson disease Causative agent Alpha-synuclein false Inferred relationship Existential restriction modifier 1
Autosomal dominant late onset Parkinson disease Interprets Movement true Inferred relationship Existential restriction modifier 3
Autosomal dominant late onset Parkinson 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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