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405809000: Ocular motor apraxia Cogan type (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
2157583012 Oculomotor apraxia - Cogan type en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
5045004019 Ocular motor apraxia Cogan type (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
5045005018 Ocular motor apraxia Cogan type en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
5045006017 Congenital saccade initiation failure en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
2149639013 Oculomotor apraxia - Cogan type (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
2157583012 Oculomotor apraxia - Cogan type en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
5045004019 Ocular motor apraxia Cogan type (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
5045005018 Ocular motor apraxia Cogan type en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
5045006017 Congenital saccade initiation failure en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
610621000274110 Okulomotorische Apraxie Typ Cogan de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
3388831001000117 Apraxie, okulomotorische, Typ Cogan de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
968381000172111 apraxie oculomotrice type Cogan fr Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
968381000172111 apraxie oculomotrice type Cogan fr Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
610621000274110 Okulomotorische Apraxie Typ Cogan de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
3388831001000117 Apraxie, okulomotorische, Typ Cogan de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module

0 descendants.

Expanded Value Set

Outbound Relationships Type Target Active Characteristic Refinability Group Values
Ocular motor apraxia Cogan type (disorder) Is a Oculomotor apraxia (disorder) true Inferred relationship Existential restriction modifier (core metadata concept)
Ocular motor apraxia Cogan type (disorder) Finding site Eye region structure false Inferred relationship Existential restriction modifier (core metadata concept) 1
Ocular motor apraxia Cogan type (disorder) Associated morphology Misalignment (morphologic abnormality) false Inferred relationship Existential restriction modifier (core metadata concept) 1
Ocular motor apraxia Cogan type (disorder) Interprets Ocular muscle balance false Inferred relationship Existential restriction modifier (core metadata concept) 1
Ocular motor apraxia Cogan type (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
Ocular motor apraxia Cogan type (disorder) Interprets Ocular motility observable (observable entity) false Inferred relationship Existential restriction modifier (core metadata concept)
Ocular motor apraxia Cogan type (disorder) Has interpretation Abnormal false Inferred relationship Existential restriction modifier (core metadata concept) 1
Ocular motor apraxia Cogan type (disorder) Interprets Ocular muscle balance false Inferred relationship Existential restriction modifier (core metadata concept) 1
Ocular motor apraxia Cogan type (disorder) Has interpretation Abnormal false Inferred relationship Existential restriction modifier (core metadata concept) 1
Ocular motor apraxia Cogan type (disorder) Is a Hereditary disorder of the visual system (disorder) true Inferred relationship Existential restriction modifier (core metadata concept)
Ocular motor apraxia Cogan type (disorder) Is a Autosomal recessive hereditary disorder true Inferred relationship Existential restriction modifier (core metadata concept)
Ocular motor apraxia Cogan type (disorder) Occurrence Congenital true Inferred relationship Existential restriction modifier (core metadata concept) 1
Ocular motor apraxia Cogan type (disorder) Is a Congenital anomaly of visual system true Inferred relationship Existential restriction modifier (core metadata concept)
Ocular motor apraxia Cogan type (disorder) Is a Developmental hereditary disorder true Inferred relationship Existential restriction modifier (core metadata concept)
Ocular motor apraxia Cogan type (disorder) Associated morphology Morphologically abnormal structure true Inferred relationship Existential restriction modifier (core metadata concept) 1
Ocular motor apraxia Cogan type (disorder) Pathological process (attribute) Pathological developmental process (qualifier value) true Inferred relationship Existential restriction modifier (core metadata concept) 1
Inbound Relationships Type Active Source Characteristic Refinability Group
Cortical paralysis of fixation syndrome Is a False Ocular motor apraxia Cogan type (disorder) Inferred relationship Existential restriction modifier (core metadata concept)

This concept is not in any reference sets

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