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193662007: Oculomotor apraxia (disorder)

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

Descriptions:

Id Description Lang Type Status Case? Module
298188010 Oculomotor apraxia en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
2147497010 Oculomotor apraxia (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
2535852016 Oculomotor dyspraxia en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
298188010 Oculomotor apraxia en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
298188010 Oculomotor apraxia en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
577566018 Oculomotor apraxia en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
2147497010 Oculomotor apraxia (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
2147497010 Oculomotor apraxia (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
2535852016 Oculomotor dyspraxia en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
2535852016 Oculomotor dyspraxia en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
632201000274110 Okulomotorische Dyspraxie de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
632211000274112 Okulomotorische Apraxie de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
887691000172112 apraxie oculomotrice fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
887691000172112 apraxie oculomotrice fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
632201000274110 Okulomotorische Dyspraxie de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
632211000274112 Okulomotorische Apraxie de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module

11 descendants. Search Descendants:

Expanded Value Set

Outbound Relationships Type Target Active Characteristic Refinability Group Values
Oculomotor apraxia (disorder) Is a Strabismus true Inferred relationship Existential restriction modifier (core metadata concept)
Oculomotor apraxia (disorder) Finding site Eye region structure false Inferred relationship Existential restriction modifier (core metadata concept) 1
Oculomotor apraxia (disorder) Associated morphology Misalignment (morphologic abnormality) false Inferred relationship Existential restriction modifier (core metadata concept) 1
Oculomotor apraxia (disorder) Interprets Ocular motility observable (observable entity) false Inferred relationship Existential restriction modifier (core metadata concept)
Oculomotor apraxia (disorder) Has interpretation Abnormal false Inferred relationship Existential restriction modifier (core metadata concept) 1
Oculomotor apraxia (disorder) Interprets Ocular muscle balance false Inferred relationship Existential restriction modifier (core metadata concept) 1
Oculomotor apraxia (disorder) Finding site The eye, ocular adnexa, afferent visual pathways, efferent visual pathways, and pupil innervation pathways true Inferred relationship Existential restriction modifier (core metadata concept) 1
Oculomotor apraxia (disorder) Interprets Ocular muscle balance false Inferred relationship Existential restriction modifier (core metadata concept) 1
Oculomotor apraxia (disorder) Has interpretation Abnormal false Inferred relationship Existential restriction modifier (core metadata concept) 1
Inbound Relationships Type Active Source Characteristic Refinability Group
Ocular motor apraxia Cogan type (disorder) Is a True Oculomotor apraxia (disorder) Inferred relationship Existential restriction modifier (core metadata concept)
Autosomal recessive cerebellar ataxia with oculomotor apraxia type 1 (disorder) Is a True Oculomotor apraxia (disorder) Inferred relationship Existential restriction modifier (core metadata concept)
Autosomal recessive cerebellar ataxia with oculomotor apraxia type 2 (disorder) Is a True Oculomotor apraxia (disorder) Inferred relationship Existential restriction modifier (core metadata concept)
Cerebellar ataxia, intellectual disability, oculomotor apraxia, cerebellar cysts syndrome Is a True Oculomotor apraxia (disorder) Inferred relationship Existential restriction modifier (core metadata concept)
Balint syndrome Is a True Oculomotor apraxia (disorder) Inferred relationship Existential restriction modifier (core metadata concept)
Psychomotor regression, oculomotor apraxia, movement disorder, nephropathy syndrome (disorder) Is a True Oculomotor apraxia (disorder) Inferred relationship Existential restriction modifier (core metadata concept)
Acquired oculomotor apraxia Is a True Oculomotor apraxia (disorder) Inferred relationship Existential restriction modifier (core metadata concept)
Cerebellar ataxia with oculomotor apraxia type 4 Is a True Oculomotor apraxia (disorder) Inferred relationship Existential restriction modifier (core metadata concept)

Reference Sets

Concept inactivation indicator attribute value reference set (foundation metadata concept)

SAME AS association reference set (foundation metadata concept)

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