Signs & Symptoms
Based on Human Phenotype Ontology (HPO) disease-phenotype annotations.
Cervical spondylosis
HP:0008480
Osteoarthritis
HP:0002758
Spina bifida occulta
HP:0003298
Spondylolisthesis
HP:0003302
Spondylolysis
HP:0003304
Related Conditions
Cervical spondylosis with vascular compression(child)
Cervical spondylosis without myelopathy(child)
Degeneration of cervical intervertebral disc(child)
Spondylosis of cervicothoracic spine(child)
Central cord syndrome due to cervical spondylosis(child)
Posterior cord syndrome due to cervical spondylosis(child)
Osteoarthritis of cervical spine(child)
Diffuse cervicobrachial syndrome(child)
Cervicothoracic spondylosis(child)
Disorder of cervical spine(parent)
Spondylosis(parent)
Musculoskeletal disorder of the neck(parent)
Quick Facts
- SNOMED CT
- 387800004
- UMLS CUI
- C1384641
- Fully Specified Name
- Cervical spondylosis (disorder)
- Specialists
- 0
- Diagnostic Biomarkers
- 0
- HPO Phenotypes
- 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.