Signs & Symptoms
Based on Human Phenotype Ontology (HPO) disease-phenotype annotations.
Abnormal involuntary eye movements
Frequent (30-79%)HP:0012547
Abnormality of the cerebral white matter
Frequent (30-79%)HP:0002500
Ataxia
Frequent (30-79%)HP:0001251
Behavioural disorders
Frequent (30-79%)HP:0000708
Choreatic disease
Frequent (30-79%)HP:0002072
Depression
Frequent (30-79%)HP:0000716
Dystonic movements
Frequent (30-79%)HP:0001332
Epilepsy
Frequent (30-79%)HP:0001250
hyperkinetic disorder
Frequent (30-79%)HP:0000752
Inability to coordinate movements when walking
Frequent (30-79%)HP:0002066
Increased reflexes
Frequent (30-79%)HP:0001347
Irritability
Frequent (30-79%)HP:0000737
Muscle rigidity
Frequent (30-79%)HP:0002063
Neuronal loss in basal ganglia
Frequent (30-79%)HP:0200147
Oral motor hypotonia
Frequent (30-79%)HP:0030190
Progressive dementia
Frequent (30-79%)HP:0000726
Slowness of movements
Frequent (30-79%)HP:0002067
Weight loss
Frequent (30-79%)HP:0001824
Wide based walk
Frequent (30-79%)HP:0002136
Dilated cerebral ventricle
Occasional (5-29%)HP:0002119
Infratentorial atrophy
Occasional (5-29%)HP:0001272
Involuntary jerking movements
Occasional (5-29%)HP:0001336
Progressive cerebellar ataxia
Occasional (5-29%)HP:0002073
Vermian atrophy
Occasional (5-29%)HP:0006855
Related Conditions
Quick Facts
- SNOMED CT
- 230299004
- UMLS CUI
- C0751208
- Fully Specified Name
- Juvenile onset Huntington's disease (disorder)
- Specialists
- 0
- Diagnostic Biomarkers
- 0
- HPO Phenotypes
- 24
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.