supranuclear palsy, progressive

Preferred Label : supranuclear palsy, progressive;

MeSH definition : A degenerative disease of the central nervous system characterized by balance difficulties; OCULAR MOTILITY DISORDERS (supranuclear ophthalmoplegia); DYSARTHRIA; swallowing difficulties; and axial DYSTONIA. Onset is usually in the fifth decade and disease progression occurs over several years. Pathologic findings include neurofibrillary degeneration and neuronal loss in the dorsal MESENCEPHALON; SUBTHALAMIC NUCLEUS; RED NUCLEUS; pallidum; dentate nucleus; and vestibular nuclei. (From Adams et al., Principles of Neurology, 6th ed, pp1076-7);

MeSH synonym : steele-richardson-olszewski syndrome; palsy, progressive supranuclear; progressive supranuclear palsies; progressive supranuclear palsy; supranuclear palsies, progressive; steele-richardson-olszewski disease; steele richardson olszewski disease; steele richardson olszewski syndrome; richardson's syndrome; richardson syndrome;

CISMeF synonym : ophthalmoplegias, progressive supranuclear; progressive supranuclear ophthalmoplegias; supranuclear ophthalmoplegias, progressive; ophthalmoplegia, progressive supranuclear; supranuclear palsy, progressive, 1; syndrome, richardson's; syndrome, steele-richardson-olszewski;

MeSH hyponym : Supranuclear Ophthalmoplegia, Progressive; Progressive Supranuclear Ophthalmoplegia; Progressive Supranuclear Palsy 1;

Wikipedia link : https://en.wikipedia.org/wiki/Progressive supranuclear palsy;

Details

Origin ID

D013494;

UMLS CUI

C0038868;

Allowable qualifiers
- blood [MeSH Qualifier]
- cerebrospinal fluid [MeSH Qualifier]
- chemically induced [MeSH Qualifier]
- classification [MeSH Qualifier]
- complications [MeSH Qualifier]
- congenital [MeSH Qualifier]
- diagnosis [MeSH Qualifier]
- diagnostic imaging [MeSH Qualifier]
- diet therapy [MeSH Qualifier]
- drug therapy [MeSH Qualifier]
- economics [MeSH Qualifier]
- embryology [MeSH Qualifier]
- enzymology [MeSH Qualifier]
- epidemiology [MeSH Qualifier]
- ethnology [MeSH Qualifier]
- etiology [MeSH Qualifier]
- genetics [MeSH Qualifier]
- history [MeSH Qualifier]
- immunology [MeSH Qualifier]
- metabolism [MeSH Qualifier]
- microbiology [MeSH Qualifier]
- mortality [MeSH Qualifier]
- nursing [MeSH Qualifier]
- parasitology [MeSH Qualifier]
- pathology [MeSH Qualifier]
- physiopathology [MeSH Qualifier]
- prevention and control [MeSH Qualifier]
- psychology [MeSH Qualifier]
- radiotherapy [MeSH Qualifier]
- rehabilitation [MeSH Qualifier]
- surgery [MeSH Qualifier]
- therapy [MeSH Qualifier]
- urine [MeSH Qualifier]
- veterinary [MeSH Qualifier]
- virology [MeSH Qualifier]
Automatic exact mappings (from CISMeF team)
- Classic progressive supranuclear palsy syndrome [ORDO Disease]
- Lithostathine-1-Alpha [NCIt concept]
- MSMB wt Allele [NCIt concept]
- Phenol red [ICD-11 Extension code]
- Pneumothorax, primary spontaneous [OMIM Phenotype]
- Progressive supranuclear palsy (disorder) [SNOMED CT concept]
- REG1A wt Allele [NCIt concept]
- Supranuclear ophthalmoplegia [PASCAL descriptor]
- Supranuclear ophthalmoplegia [HPO term]
Currated CISMeF NLP mapping
- Progressive Supranuclear Palsy [NCIt concept]
- 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 [DO Concept]
- progressive supranuclear palsy [Disease (Nov.)]
- progressive supranuclear palsy [MedlinePlus Topic]
- progressive supranuclear palsy [Radlex concept]
DO Cross reference
- progressive supranuclear palsy [DO Concept]
Manual BTNT mappings - CISMeF
- Atypical progressive supranuclear palsy syndrome [ORDO Disease]
Manual NTBT mappings (CISMeF)
- Genetic neurodegenerative disease [ORDO Disease]
- Neurodegenerative disease with dementia [ORDO Disease]
- Rare dementia [ORDO Disease]
- Rare genetic movement disorder [ORDO Disease]
- Rare movement disorder [ORDO Disease]
- Rare neurodegenerative disease [ORDO Disease]
- Supranuclear eye movement disorder [ORDO Disease]
- Tauopathy with a major tau doublet at 64 and 69 kDa [ORDO Disease]
MedlinePlus topic(s)
- progressive supranuclear palsy [MedlinePlus Topic]
ORDO relation(s)
- Progressive supranuclear palsy [ORDO Disease]
Record concept(s)
- Ophthalmoplegia, Progressive Supranuclear [MeSH concept]
- Supranuclear Palsy, Progressive, 1 [MeSH concept]
- supranuclear palsy, progressive [MeSH concept]
Related MeSH Supplementary Concept(s)
- familial progressive supranuclear palsy [MeSH Supplementary Concept]
- progressive supranuclear palsy atypical [MeSH Supplementary Concept]
- supranuclear palsy, progressive, 2 [MeSH Supplementary Concept]
- supranuclear palsy, progressive, 3 [MeSH Supplementary Concept]
- tauopathy and respiratory failure [MeSH Supplementary Concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Classic progressive supranuclear palsy syndrome [ORDO Disease]
- Progressive Supranuclear Palsy [NCIt concept]
- 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]

Keyword's position in hierarchy(ies) :

Main resources

You can consult :

recommendations
documents concerning education
documents for patients