Signs & Symptoms
Based on Human Phenotype Ontology (HPO) disease-phenotype annotations.
Jerking
Very frequent (80-99%)HP:0001336
Parkinsonian disease
Very frequent (80-99%)HP:0001300
Progressive extrapyramidal muscular rigidity
Very frequent (80-99%)HP:0007158
Akinesia
Frequent (30-79%)HP:0002304
Frontal release signs
Frequent (30-79%)HP:0000743
Gait disturbance
Frequent (30-79%)HP:0001288
Imbalance
Frequent (30-79%)HP:0002172
Involuntary movements
Frequent (30-79%)HP:0004305
Limb apraxia
Frequent (30-79%)HP:0030217
Limb dystonia
Frequent (30-79%)HP:0002451
Myoclonus of limbs
Frequent (30-79%)HP:0045084
Oromotor apraxia
Frequent (30-79%)HP:0007301
Progressive dementia
Frequent (30-79%)HP:0000726
Sensory impairment
Frequent (30-79%)HP:0003474
Slowness of movements
Frequent (30-79%)HP:0002067
Tremor
Frequent (30-79%)HP:0001337
Difficulty finding words
Occasional (5-29%)HP:0002381
Dystonic movements
Occasional (5-29%)HP:0001332
Memory loss
Occasional (5-29%)HP:0002354
Verbal dyspraxia
Occasional (5-29%)HP:0011098
Abnormality of movement
Very rare (1-4%)HP:0100022
Behavioural disorders
Very rare (1-4%)HP:0000708
Quick Facts
- SNOMED CT
- 18842008
- UMLS CUI
- C0393570
- Fully Specified Name
- Corticobasal degeneration (disorder)
- Specialists
- 0
- Diagnostic Biomarkers
- 0
- HPO Phenotypes
- 22
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.