Overview
Hemidystonia hemiatrophy 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.
Abnormal basal ganglia MRI signal intensity
Very frequent (80-99%)HP:0012751
Abnormality of the periventricular white matter
Very frequent (80-99%)HP:0002518
Dystonic movements
Very frequent (80-99%)HP:0001332
Hemiparesis
Very frequent (80-99%)HP:0001269
Abnormal delivery
Frequent (30-79%)HP:0001787
Asymmetric limb shortening
Frequent (30-79%)HP:0100556
Limb dystonia
Frequent (30-79%)HP:0002451
Abnormal paranasal sinus morphology
Occasional (5-29%)HP:0000245
Advanced pneumatization of cranial sinuses
Occasional (5-29%)HP:0010540
Corticospinal signs
Occasional (5-29%)HP:0007256
Dense skull cap
Occasional (5-29%)HP:0000250
Epilepsy
Occasional (5-29%)HP:0001250
Extensor plantar responses
Occasional (5-29%)HP:0003487
Delayed motor milestones
Very rare (1-4%)HP:0001270
Rhizomelic leg shortening
Very rare (1-4%)HP:0012106
Related Conditions
Quick Facts
- SNOMED CT
- 724383002
- UMLS CUI
- C4510649
- Fully Specified Name
- Hemidystonia hemiatrophy syndrome (disorder)
- Specialists
- 0
- Diagnostic Biomarkers
- 0
- HPO Phenotypes
- 15
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.