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59103002: Cerebral paralysis with homolateral ataxia (disorder)


Status: current, Primitive. Date: 31-Jan 2002. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
797909011 Cerebral paralysis with homolateral ataxia (disorder) en Fully specified name Active Case insensitive SNOMED CT core
98215013 Cerebral paralysis with homolateral ataxia en Synonym Active Case insensitive SNOMED CT core


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Cerebral paralysis with homolateral ataxia Associated morphology Degenerative abnormality true Inferred relationship Some 1
Cerebral paralysis with homolateral ataxia Interprets Movement true Inferred relationship Some 3
Cerebral paralysis with homolateral ataxia Interprets Movement observable true Inferred relationship Some 2
Cerebral paralysis with homolateral ataxia Has interpretation Absent true Inferred relationship Some 2
Cerebral paralysis with homolateral ataxia Finding site Brain structure false Inferred relationship Some 1
Cerebral paralysis with homolateral ataxia Is a Cerebral ataxia true Inferred relationship Some
Cerebral paralysis with homolateral ataxia Is a Paralytic syndrome true Inferred relationship Some
Cerebral paralysis with homolateral ataxia Finding site Brain structure true Inferred relationship Some 1
Cerebral paralysis with homolateral ataxia Associated morphology Degeneration false Inferred relationship Some 1
Cerebral paralysis with homolateral ataxia Finding site Structure of cerebral cortex false Inferred relationship Some
Cerebral paralysis with homolateral ataxia Finding site Structure of central nervous system false Inferred relationship Some 2
Cerebral paralysis with homolateral ataxia Associated morphology Degeneration false Inferred relationship Some 1

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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