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765212008: Balint syndrome (disorder)


Status: current, Primitive. Date: 31-Jul 2018. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
3657467019 Optic ataxia, gaze apraxia, simultanagnosia syndrome en Synonym Active Case insensitive SNOMED CT core
3657468012 Balint syndrome en Synonym Active Case sensitive SNOMED CT core
3657469016 Balint Holmes syndrome en Synonym Active Case sensitive SNOMED CT core
3657470015 Balint syndrome (disorder) en Fully specified name Active Case sensitive SNOMED CT core
3657471016 A rare neurologic disease with characteristics of the triad of optic ataxia, ocular apraxia and simultanagnosia due to posterior parietal lobe lesions. Patients report ophthalmologic difficulties in the absence of underlying ophthalmologic anomalies and present severe visual and spatial disabilities in locating and reaching objects, initiating voluntary eye movements and perceiving more than one object at a time. en Definition Active Case sensitive SNOMED CT core


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Balint syndrome Is a Neurological disorder true Inferred relationship Some
Balint syndrome Finding site Structure of nervous system true Inferred relationship Some 1
Balint syndrome Is a Oculomotor apraxia true Inferred relationship Some
Balint syndrome Finding site Structure of visual system true Inferred relationship Some 2

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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