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278512001: Ataxic cerebral palsy (disorder)


Status: current, Sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jul 2014. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
415444017 Ataxic cerebral palsy en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
671678018 Ataxic cerebral palsy (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
2995485017 Ataxic infantile cerebral palsy en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
2995945017 A subtype of non-spastic cerebral palsy with loss of muscular coordination with abnormal force and rhythm, and impairment of accuracy; commonly presents with gait and trunk ataxia, poor balance, past pointing, terminal intention tremor, scanning speech, nystagmus and other abnormal eye movements, and hypotonia. Low tone is a prominent feature. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
415444017 Ataxic cerebral palsy en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
415444017 Ataxic cerebral palsy en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
671678018 Ataxic cerebral palsy (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
671678018 Ataxic cerebral palsy (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
2995485017 Ataxic infantile cerebral palsy en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
2995485017 Ataxic infantile cerebral palsy en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
2995945017 A subtype of non-spastic cerebral palsy with loss of muscular coordination with abnormal force and rhythm, and impairment of accuracy; commonly presents with gait and trunk ataxia, poor balance, past pointing, terminal intention tremor, scanning speech, nystagmus and other abnormal eye movements, and hypotonia. Low tone is a prominent feature. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
259851000172114 paralysie cérébrale ataxique fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
259851000172114 paralysie cérébrale ataxique fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
A subtype of non-spastic cerebral palsy with loss of muscular coordination with abnormal force and rhythm, and impairment of accuracy; commonly presents with gait and trunk ataxia, poor balance, past pointing, terminal intention tremor, scanning speech, nystagmus and other abnormal eye movements, and hypotonia. Low tone is a prominent feature. Is a Infantile spastic cerebral palsy false Inferred relationship Existential restriction modifier (core metadata concept)
A subtype of non-spastic cerebral palsy with loss of muscular coordination with abnormal force and rhythm, and impairment of accuracy; commonly presents with gait and trunk ataxia, poor balance, past pointing, terminal intention tremor, scanning speech, nystagmus and other abnormal eye movements, and hypotonia. Low tone is a prominent feature. Finding site The cerebrum is the regional structure of the brain, which is the adult equivalent of the forebrain or prosencephalon. It is constituted by the structural derivatives of the telencephalon and diencephalon including the cerebral hemispheres, epithalamus, thalamus, hypothalamus, lateral ventricles and third ventricle. This definition is harmonious with the Federation of Association of Anatomist Second Edition (2019) Part V Terminologia Anatomica. true Inferred relationship Existential restriction modifier (core metadata concept) 1
A subtype of non-spastic cerebral palsy with loss of muscular coordination with abnormal force and rhythm, and impairment of accuracy; commonly presents with gait and trunk ataxia, poor balance, past pointing, terminal intention tremor, scanning speech, nystagmus and other abnormal eye movements, and hypotonia. Low tone is a prominent feature. Finding site Extrapyramidal system structure true Inferred relationship Existential restriction modifier (core metadata concept) 2
A subtype of non-spastic cerebral palsy with loss of muscular coordination with abnormal force and rhythm, and impairment of accuracy; commonly presents with gait and trunk ataxia, poor balance, past pointing, terminal intention tremor, scanning speech, nystagmus and other abnormal eye movements, and hypotonia. Low tone is a prominent feature. Is a Ataxia true Inferred relationship Existential restriction modifier (core metadata concept)
A subtype of non-spastic cerebral palsy with loss of muscular coordination with abnormal force and rhythm, and impairment of accuracy; commonly presents with gait and trunk ataxia, poor balance, past pointing, terminal intention tremor, scanning speech, nystagmus and other abnormal eye movements, and hypotonia. Low tone is a prominent feature. Is a A less common type of cerebral palsy defined by decreased and/or fluctuating muscle tone; multiple forms of non-spastic cerebral palsy are each characterised by particular impairments; one of the main characteristics of non-spastic cerebral palsy is involuntary movement. Subtypes include ataxic and dyskinetic forms. true Inferred relationship Existential restriction modifier (core metadata concept)
A subtype of non-spastic cerebral palsy with loss of muscular coordination with abnormal force and rhythm, and impairment of accuracy; commonly presents with gait and trunk ataxia, poor balance, past pointing, terminal intention tremor, scanning speech, nystagmus and other abnormal eye movements, and hypotonia. Low tone is a prominent feature. Clinical course Non-progressive (qualifier value) true Inferred relationship Existential restriction modifier (core metadata concept) 3
A subtype of non-spastic cerebral palsy with loss of muscular coordination with abnormal force and rhythm, and impairment of accuracy; commonly presents with gait and trunk ataxia, poor balance, past pointing, terminal intention tremor, scanning speech, nystagmus and other abnormal eye movements, and hypotonia. Low tone is a prominent feature. Interprets Movement true Inferred relationship Existential restriction modifier (core metadata concept) 4
A subtype of non-spastic cerebral palsy with loss of muscular coordination with abnormal force and rhythm, and impairment of accuracy; commonly presents with gait and trunk ataxia, poor balance, past pointing, terminal intention tremor, scanning speech, nystagmus and other abnormal eye movements, and hypotonia. Low tone is a prominent feature. Interprets Movement observable true Inferred relationship Existential restriction modifier (core metadata concept) 5
A subtype of non-spastic cerebral palsy with loss of muscular coordination with abnormal force and rhythm, and impairment of accuracy; commonly presents with gait and trunk ataxia, poor balance, past pointing, terminal intention tremor, scanning speech, nystagmus and other abnormal eye movements, and hypotonia. Low tone is a prominent feature. Has interpretation Absent true Inferred relationship Existential restriction modifier (core metadata concept) 5

Inbound Relationships Type Active Source Characteristic Refinability Group
Ataxic infantile cerebral palsy Is a False A subtype of non-spastic cerebral palsy with loss of muscular coordination with abnormal force and rhythm, and impairment of accuracy; commonly presents with gait and trunk ataxia, poor balance, past pointing, terminal intention tremor, scanning speech, nystagmus and other abnormal eye movements, and hypotonia. Low tone is a prominent feature. Inferred relationship Existential restriction modifier (core metadata concept)

This concept is not in any reference sets

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