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193662007: Oculomotor apraxia (disorder)

Status: current, Not sufficiently defined by necessary conditions definition status. Date: 31-Jan 2004. Module: SNOMED CT core module

Descriptions:

Id Description Lang Type Status Case? Module
298188010 Oculomotor apraxia en Synonym Active Entire term case insensitive SNOMED CT core module
2147497010 Oculomotor apraxia (disorder) en Fully specified name Active Entire term case insensitive SNOMED CT core module
2535852016 Oculomotor dyspraxia en Synonym Active Entire term case insensitive SNOMED CT core module
345231000000117 Oculomotor apraxia (& Cogan) en Synonym Active Only initial character case insensitive SNOMED CT United Kingdom Edition module

11 descendants. Search Descendants:

Expanded Value Set

Outbound Relationships Type Target Active Characteristic Refinability Group Values
Oculomotor apraxia Is a Strabismus true Inferred relationship Existential restriction modifier
Oculomotor apraxia Finding site Eye region structure false Inferred relationship Existential restriction modifier 1
Oculomotor apraxia Associated morphology Misalignment false Inferred relationship Existential restriction modifier 1
Oculomotor apraxia Interprets Ocular motility observable false Inferred relationship Existential restriction modifier
Oculomotor apraxia Has interpretation Abnormal false Inferred relationship Existential restriction modifier 1
Oculomotor apraxia Interprets Ocular muscle balance false Inferred relationship Existential restriction modifier 1
Oculomotor apraxia Finding site Structure of visual system true Inferred relationship Existential restriction modifier 1
Oculomotor apraxia Interprets Ocular muscle balance false Inferred relationship Existential restriction modifier 1
Oculomotor apraxia Has interpretation Abnormal false Inferred relationship Existential restriction modifier 1
Inbound Relationships Type Active Source Characteristic Refinability Group
Ocular motor apraxia Cogan type Is a True Oculomotor apraxia Inferred relationship Existential restriction modifier
Autosomal recessive cerebellar ataxia with oculomotor apraxia type 1 Is a True Oculomotor apraxia Inferred relationship Existential restriction modifier
Autosomal recessive cerebellar ataxia with oculomotor apraxia type 2 Is a True Oculomotor apraxia Inferred relationship Existential restriction modifier
Cerebellar ataxia, intellectual disability, oculomotor apraxia, cerebellar cysts syndrome Is a True Oculomotor apraxia Inferred relationship Existential restriction modifier
Balint syndrome Is a True Oculomotor apraxia Inferred relationship Existential restriction modifier
Psychomotor regression, oculomotor apraxia, movement disorder, nephropathy syndrome Is a True Oculomotor apraxia Inferred relationship Existential restriction modifier
Acquired oculomotor apraxia Is a True Oculomotor apraxia Inferred relationship Existential restriction modifier
Cerebellar ataxia with oculomotor apraxia type 4 Is a True Oculomotor apraxia Inferred relationship Existential restriction modifier

This concept is not in any reference sets

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