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Progressive supranuclear palsy corticobasal syndrome
disorderSNOMED 1156763004CUI C5548189
Overview
Progressive supranuclear palsy corticobasal syndrome is a disorder.
Auto-generated from clinical reference data. Not a substitute for medical advice.
Signs & Symptoms
Based on Human Phenotype Ontology (HPO) disease-phenotype annotations.
Slowness of movements
Always present (100%)HP:0002067
Abnormal retropulsion test
Very frequent (80-99%)HP:0002172
Apraxia
Very frequent (80-99%)HP:0002186
Corticospinal signs
Very frequent (80-99%)HP:0007256
Focal dystonia
Very frequent (80-99%)HP:0004373
Limb apraxia
Very frequent (80-99%)HP:0030217
Slow visual tracking
Very frequent (80-99%)HP:0000514
Abnormal saccadic eye movements
Frequent (30-79%)HP:0000570
Difficulty articulating speech
Frequent (30-79%)HP:0001260
Difficulty finding words
Frequent (30-79%)HP:0002381
Diminished movement
Frequent (30-79%)HP:0002374
Frequent falls
Frequent (30-79%)HP:0002359
Intellectual deterioration
Frequent (30-79%)HP:0001268
Involuntary movements
Frequent (30-79%)HP:0004305
Memory impairment
Frequent (30-79%)HP:0002354
Muscle rigidity
Frequent (30-79%)HP:0002063
Myoclonus of limbs
Frequent (30-79%)HP:0045084
Progressive extrapyramidal muscular rigidity
Frequent (30-79%)HP:0007158
Sensory impairment
Frequent (30-79%)HP:0003474
Slowed horizontal saccades
Frequent (30-79%)HP:0007885
Thumb clasp
Frequent (30-79%)HP:0001188
Tremor
Frequent (30-79%)HP:0001337
VSGP
Frequent (30-79%)HP:0000511
Deglutition disorder
Occasional (5-29%)HP:0002015
Jerky head movements
Occasional (5-29%)HP:0006961
Parkinsonism with favorable response to dopaminergic medication
Occasional (5-29%)HP:0002548
Personality changes
Occasional (5-29%)HP:0000751
Speech articulation difficulties
Occasional (5-29%)HP:0009088
Laboured breathing
Very rare (1-4%)HP:0002098
Related Conditions
Quick Facts
- SNOMED CT
- 1156763004
- UMLS CUI
- C5548189
- Fully Specified Name
- Progressive supranuclear palsy corticobasal syndrome (disorder)
- Specialists
- 0
- Diagnostic Biomarkers
- 0
- HPO Phenotypes
- 29
Medical Disclaimer
This information is for educational purposes only and does not constitute medical advice, diagnosis, or treatment. Always consult with a qualified healthcare provider regarding any medical condition or treatment plan.
Clinical content is derived from the SNOMED CT clinical ontology and curated medical knowledge graphs.