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1156822001: Autosomal recessive familial Parkinson disease (disorder)


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

Descriptions:

Id Description Lang Type Status Case? Module
4576267016 Autosomal recessive familial Parkinson disease en Synonym Active Only initial character case insensitive SNOMED CT core module
4576268014 Autosomal recessive familial Parkinson disease (disorder) en Fully specified name 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 recessive familial Parkinson disease Associated morphology Degenerative abnormality true Inferred relationship Existential restriction modifier 1
Autosomal recessive familial Parkinson disease Is a Parkinson's disease true Inferred relationship Existential restriction modifier
Autosomal recessive familial Parkinson disease Is a Hereditary degenerative disease of central nervous system true Inferred relationship Existential restriction modifier
Autosomal recessive familial Parkinson disease Causative agent Alpha-synuclein false Inferred relationship Existential restriction modifier 1
Autosomal recessive familial Parkinson disease Is a Autosomal recessive hereditary disorder true Inferred relationship Existential restriction modifier
Autosomal recessive familial Parkinson disease Finding site Basal ganglion structure true Inferred relationship Existential restriction modifier 1
Autosomal recessive familial Parkinson disease Interprets Movement true Inferred relationship Existential restriction modifier 3
Autosomal recessive familial 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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