Progressive Supranuclear Palsy

Preferred Label : Progressive Supranuclear Palsy;

NCIt synonyms : Steele-Richardson-Olszewski Syndrome;

NCIt related terms : Progressive supranuclear ophthalmoplegia;

NCIt definition : A rare neurodegenerative disorder characterized by gait and balance difficulties and loss of coordination of eye movements.;

Codes from synonyms : G23.1;

Details

Origin ID

C85028;

UMLS CUI

C0038868;

Automatic exact mappings (from CISMeF team)
- Progressive supranuclear palsy (disorder) [SNOMED CT concept]
Currated CISMeF NLP mapping
- Progressive supranuclear ophthalmoplegia [ICD-10 Sub-category (who)]
- Progressive supranuclear ophthalmoplegia (disorder) [SNOMED CT concept]
- Progressive supranuclear ophthalmoplegia [Steele-Richardson-Olszewski] [ICD-10 Sub-category]
- Progressive supranuclear palsy [ICD-11 Sub-sub category]
- Progressive supranuclear palsy [MedDRA Preferred Term]
- Progressive supranuclear palsy [ORDO Disease]
- Steele-Richardson-Olszewski syndrome [MedDRA LLT]
- Supranuclear palsy, progressive, 1 [OMIM Phenotype]
- progressive supranuclear ophthalmoplegia [SNOMED Notion]
- progressive supranuclear palsy [Radlex concept]
- progressive supranuclear palsy [DO Concept]
- progressive supranuclear palsy [Disease (Nov.)]
- progressive supranuclear palsy [MedlinePlus Topic]
- supranuclear palsy, progressive [MeSH Descriptor]
- supranuclear palsy, progressive [MeSH concept]
DO Cross reference
- progressive supranuclear palsy [DO Concept]
Has associated anatomic sites
- Central Nervous System [NCIt concept]
- Nervous System [NCIt concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Classic progressive supranuclear palsy syndrome [ORDO Disease]
- Progressive supranuclear ophthalmoplegia [ICD-10 Sub-category (who)]
- Progressive supranuclear palsy [ORDO Disease]
- Progressive supranuclear palsy [MedDRA Preferred Term]
- Progressive supranuclear palsy (disorder) [SNOMED CT concept]
- Steele-Richardson-Olszewski syndrome [MedDRA LLT]
- Supranuclear palsy, progressive, 1 [OMIM Phenotype]
- progressive supranuclear ophthalmoplegia [SNOMED Notion]
- progressive supranuclear palsy [Radlex concept]
- progressive supranuclear palsy [DO Concept]
- progressive supranuclear palsy [MedlinePlus Topic]
- supranuclear palsy, progressive [MeSH concept]
- supranuclear palsy, progressive [MeSH Descriptor]
concept_is_in_subset
- Cellosaurus Disease Terminology [NCIt concept]
- mCode Elixhauser Neurological Movement Disorder Value Set [NCIt concept]
- mCode Terminology [NCIt concept]
disease_has_finding
- Rare Lesion [NCIt concept]
disease_has_primary_anatomic_site
- Central Nervous System [NCIt concept]
- Nervous System [NCIt concept]
related_to_genetic_biomarker
- MAPT Gene [NCIt concept]

Keyword's position in hierarchy(ies) :

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