193662007: Oculomotor apraxia (disorder)

SNOMED CT Concept\Clinical finding\...

\Eye / vision finding\Visual system disorder\Disorder of eye movements\Strabismus\Oculomotor apraxia

\Disease\Disorder of body system\Visual system disorder\Disorder of eye movements\Strabismus\Oculomotor apraxia

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
577566018 Oculomotor apraxia en Fully specified name Inactive Only initial character 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

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