Overview
Camptocormia 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.
Abnormality of the cerebral white matter
Frequent (30-79%)HP:0002500
Abnormality of the intervertebral disc
Frequent (30-79%)HP:0005108
Abnormality of the nervous system
Frequent (30-79%)HP:0000707
Cerebral atrophy
Frequent (30-79%)HP:0002059
Dystonic movements
Frequent (30-79%)HP:0001332
EMG: impaired neuromuscular transmission
Frequent (30-79%)HP:0100285
EMG: myopathic changes
Frequent (30-79%)HP:0003458
EMG: neuropathic changes
Frequent (30-79%)HP:0003445
Osteoarthritis
Frequent (30-79%)HP:0002758
Abnormal head
Occasional (5-29%)HP:0000234
Abnormal inflammatory response
Occasional (5-29%)HP:0012647
Abnormality of movement
Occasional (5-29%)HP:0100022
Amyotrophic lateral sclerosis
Occasional (5-29%)HP:0007354
Elevated circulating creatine phosphokinase
Occasional (5-29%)HP:0003236
EMG: chronic denervation signs
Occasional (5-29%)HP:0003444
Parkinsonian disease
Occasional (5-29%)HP:0001300
Proximal spinal muscular atrophy
Occasional (5-29%)HP:0006959
Abnormal muscle fiber dysferlin
Very rare (1-4%)HP:0030113
Abnormal pons morphology
Very rare (1-4%)HP:0007361
Abnormality of neuromuscular transmission
Very rare (1-4%)HP:0003398
Abnormality of the basal ganglia
Very rare (1-4%)HP:0002134
Alzheimer disease
Very rare (1-4%)HP:0002511
Delayed relaxation of muscle fibres after contraction
Very rare (1-4%)HP:0002486
Fatigable weakness of skeletal muscles
Very rare (1-4%)HP:0030197
Fatty replacement of skeletal muscle
Very rare (1-4%)HP:0012548
Fluid-filled cyst in spinal cord
Very rare (1-4%)HP:0003396
Frontotemporal dementia
Very rare (1-4%)HP:0002145
Immunological abnormality
Very rare (1-4%)HP:0002715
Inflammation of spinal cord
Very rare (1-4%)HP:0012486
Lewy body disease
Very rare (1-4%)HP:0100315
Related Conditions
Quick Facts
- SNOMED CT
- 13534001
- UMLS CUI
- C0264162
- Fully Specified Name
- Camptocormia (disorder)
- Specialists
- 0
- Diagnostic Biomarkers
- 0
- HPO Phenotypes
- 30
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.