Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2018. Module: SNOMED CT core
Descriptions:
| Id | Description | Lang | Type | Status | Case? | Module |
| 297258013 | Progressive supranuclear palsy | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 2721920017 | Progressive supranuclear palsy (disorder) | en | Fully specified name | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 3511377010 | PSP - progressive supranuclear palsy | en | Synonym (core metadata concept) | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
| 6773781000146114 | progressieve supranucleaire verlamming | nl | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT Netherlands NRC maintained module (core metadata concept) |
| 6773791000146111 | PSP | nl | Synonym (core metadata concept) | Active | Entire term case sensitive (core metadata concept) | SNOMED CT Netherlands NRC maintained module (core metadata concept) |
| 6773801000146110 | progressieve supranucleaire verlamming (aandoening) | nl | Fully specified name | Active | Entire term case insensitive (core metadata concept) | SNOMED CT Netherlands NRC maintained module (core metadata concept) |
| 7097671000146119 | progressieve supranucleaire paralyse | nl | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT Netherlands NRC maintained module (core metadata concept) |
| 3511375019 | 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. | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
| 7742441000146118 | Progressieve supranucleaire paralyse (PSP) is een aandoening die lijkt op de ziekte van Parkinson, echter zonder beverigheid. Kenmerken zijn stijfheid en verminderde beweeglijkheid, stoornissen in oogbewegingen en uiteindelijk dementie. | nl | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT Netherlands NRC maintained module (core metadata concept) |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
| Atypical progressive supranuclear palsy syndrome | Is a | True | Progressive supranuclear palsy | Inferred relationship | Some | |
| Classic progressive supranuclear palsy syndrome (disorder) | Is a | True | Progressive supranuclear palsy | Inferred relationship | Some |
This concept is not in any reference sets
FHIR