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1156822001: autosomaal recessieve familiaire ziekte van Parkinson (aandoening)


Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jul 2021. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
4576267016 Autosomal recessive familial Parkinson disease en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
4576268014 Autosomal recessive familial Parkinson disease (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
12891741000146110 autosomaal recessieve familiaire ziekte van Parkinson nl Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT Netherlands NRC maintained module (core metadata concept)
12891751000146113 autosomaal recessieve familiaire ziekte van Parkinson (aandoening) nl Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT Netherlands NRC maintained module (core metadata concept)


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Autosomal recessive familial Parkinson disease Associated morphology Degenerative abnormality true Inferred relationship Some 1
Autosomal recessive familial Parkinson disease Is a Parkinson's disease true Inferred relationship Some
Autosomal recessive familial Parkinson disease Is a Hereditary degenerative disease of central nervous system true Inferred relationship Some
Autosomal recessive familial Parkinson disease Causative agent Alpha-synuclein false Inferred relationship Some 1
Autosomal recessive familial Parkinson disease Is a Autosomal recessive hereditary disorder true Inferred relationship Some
Autosomal recessive familial Parkinson disease Finding site Basal ganglion structure (body structure) true Inferred relationship Some 1
Autosomal recessive familial Parkinson disease Interprets Movement true Inferred relationship Some 3
Autosomal recessive familial Parkinson disease Has interpretation Slow true Inferred relationship Some 3
Autosomal recessive familial Parkinson disease Clinical course Progressive (qualifier value) true Inferred relationship Some 2

Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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