Overview
O'Sullivan McLeod 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 electromyography finding
Very frequent (80-99%)HP:0003457
Hand muscle weakness
Very frequent (80-99%)HP:0030237
Intrinsic hand muscle atrophy
Very frequent (80-99%)HP:0008954
Upper limb muscle weakness
Very frequent (80-99%)HP:0003484
Cold paresis
Frequent (30-79%)HP:0031372
Degeneration of the spinal cord
Frequent (30-79%)HP:0006827
EMG: chronic denervation signs
Frequent (30-79%)HP:0003444
Muscle fasciculation
Frequent (30-79%)HP:0002380
Pain
Frequent (30-79%)HP:0012531
Tremor
Frequent (30-79%)HP:0001337
Elevated immunoglobulin levels
Occasional (5-29%)HP:0010702
Eosinophilia
Occasional (5-29%)HP:0001880
Quick Facts
- SNOMED CT
- 1299151005
- UMLS CUI
- C2721741
- Fully Specified Name
- O'Sullivan McLeod syndrome (disorder)
- Specialists
- 0
- Diagnostic Biomarkers
- 0
- HPO Phenotypes
- 12
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.