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420675003: Supranuclear gaze palsy (disorder)

Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jul 2006. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
2615792016 Supranuclear gaze palsy (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
2618475013 Supranuclear gaze palsy en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
2615792016 Supranuclear gaze palsy (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
2615792016 Supranuclear gaze palsy (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
2618475013 Supranuclear gaze palsy en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
2618475013 Supranuclear gaze palsy en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
542061000274111 Supranukleäre Blickparese de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
576451000274118 Supranukleäre Blicklähmung de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
5289341000241115 paralysie du regard supranucléaire fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
5289341000241115 paralysie du regard supranucléaire fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
542061000274111 Supranukleäre Blickparese de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
576451000274118 Supranukleäre Blicklähmung de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module

5 descendants. Search Descendants:

Expanded Value Set

Outbound Relationships Type Target Active Characteristic Refinability Group Values
Supranuclear gaze palsy (disorder) Is a Neurologic disorder of eye movements (disorder) true Inferred relationship Existential restriction modifier (core metadata concept)
Supranuclear gaze palsy (disorder) Is a Supranuclear paralysis true Inferred relationship Existential restriction modifier (core metadata concept)
Supranuclear gaze palsy (disorder) Finding site Brain structure true Inferred relationship Existential restriction modifier (core metadata concept) 1
Supranuclear gaze palsy (disorder) Has interpretation Abnormal false Inferred relationship Existential restriction modifier (core metadata concept)
Supranuclear gaze palsy (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) 2
Supranuclear gaze palsy (disorder) Interprets Ocular motility observable (observable entity) false Inferred relationship Existential restriction modifier (core metadata concept)
Supranuclear gaze palsy (disorder) Interprets Movement true Inferred relationship Existential restriction modifier (core metadata concept) 4
Supranuclear gaze palsy (disorder) Interprets Movement observable true Inferred relationship Existential restriction modifier (core metadata concept) 3
Supranuclear gaze palsy (disorder) Has interpretation Absent true Inferred relationship Existential restriction modifier (core metadata concept) 3
Inbound Relationships Type Active Source Characteristic Refinability Group
A rare late-onset neurodegenerative disease with characteristics of supranuclear gaze palsy, postural instability, progressive rigidity, and mild dementia. Five clinical variants have been described with clinicopathological correlations, with Richardson's syndrome the most common clinical variant. The disease has neuropathological manifestations of neuronal loss, gliosis with astrocytic plaques and accumulation of tau-immunoreactive neurofibrillary tangles in specific brain areas. The differences in the rate and areas of accumulation of phosphorylated tau protein correlate with the five clinical variants. The disease is a 4R tauopathy composed of a preponderance of four-repeat (exon 10 positive) tau isoforms and a characteristic biochemical profile (doublet tau 64 and tau 69). The MAPT H1-clade specific sub-haplotype, H1c, is a risk factor for this disease. Is a True Supranuclear gaze palsy (disorder) Inferred relationship Existential restriction modifier (core metadata concept)

This concept is not in any reference sets

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