Treatments & Interventions
Signs & Symptoms
Based on Human Phenotype Ontology (HPO) disease-phenotype annotations.
Choreatic disease
Very frequent (80-99%)HP:0002072
Increased reflexes
Very frequent (80-99%)HP:0001347
Intellectual deterioration
Very frequent (80-99%)HP:0001268
Abnormal libido
Frequent (30-79%)HP:0031845
Abnormality of balance
Frequent (30-79%)HP:0002141
Abnormality of the sense of smell
Frequent (30-79%)HP:0004408
Agitation
Frequent (30-79%)HP:0000713
Anxiety disease
Frequent (30-79%)HP:0000739
Clumsiness
Frequent (30-79%)HP:0002312
Decreased muscle movement
Frequent (30-79%)HP:0002375
Delusions
Frequent (30-79%)HP:0000746
Depression
Frequent (30-79%)HP:0000716
Dystonic movements
Frequent (30-79%)HP:0001332
Eye movement issue
Frequent (30-79%)HP:0000496
Fine motor skill dysfunction
Frequent (30-79%)HP:0007010
Gait disturbance
Frequent (30-79%)HP:0001288
Hallucinations
Frequent (30-79%)HP:0000738
Hostile
Frequent (30-79%)HP:0031473
Impulse control disorders
Frequent (30-79%)HP:0000734
Involuntary jerking movements
Frequent (30-79%)HP:0001336
Involuntary movements
Frequent (30-79%)HP:0004305
Irritability
Frequent (30-79%)HP:0000737
Lack of feeling, emotion, interest
Frequent (30-79%)HP:0000741
Memory impairment
Frequent (30-79%)HP:0002354
Mental slowness
Frequent (30-79%)HP:0031843
Muscle weakness, generalised
Frequent (30-79%)HP:0003324
OCD
Frequent (30-79%)HP:0000722
physical aggression
Frequent (30-79%)HP:0000718
Slowness of movements
Frequent (30-79%)HP:0002067
Speech articulation difficulties
Frequent (30-79%)HP:0009088
Related Conditions
Juvenile onset Huntington's disease(child)
Late onset Huntington's disease(child)
Akinetic-rigid form of Huntington's disease(child)
Autosomal dominant hereditary disorder(parent)
Dementia(parent)
Chronic organic mental disorder(parent)
Myoneural disorder(parent)
Hereditary disorder of musculoskeletal system(parent)
Chronic musculoskeletal disorder(parent)
Dystonia(parent)
Hereditary degenerative disease of central nervous system(parent)
Atrophy of caudate nucleus(parent)
Progressive chorea(parent)
Quick Facts
- SNOMED CT
- 58756001
- UMLS CUI
- C0020179
- Fully Specified Name
- Huntington's chorea (disorder)
- Specialists
- 0
- Diagnostic Biomarkers
- 0
- HPO Phenotypes
- 30
- Known Treatments
- 5
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.