Signs & Symptoms
Based on Human Phenotype Ontology (HPO) disease-phenotype annotations.
Abnormal electromyography finding
Very frequent (80-99%)HP:0003457
Amyotrophy involving the upper limbs
Very frequent (80-99%)HP:0009129
Arthritic pain
Very frequent (80-99%)HP:0002829
Polyneuropathy
Very frequent (80-99%)HP:0001271
Upper limb muscle weakness
Very frequent (80-99%)HP:0003484
Upper limb pain
Very frequent (80-99%)HP:0012513
Paresthesia
Frequent (30-79%)HP:0003401
Scapula alata
Frequent (30-79%)HP:0003691
Sprengel deformity
Frequent (30-79%)HP:0000912
Abnormal vocalization
Occasional (5-29%)HP:0002167
Cleft of palate
Occasional (5-29%)HP:0000175
Decreased body height
Occasional (5-29%)HP:0004322
Hypoaesthesia
Occasional (5-29%)HP:0033748
Narrow mouth
Occasional (5-29%)HP:0000160
Neuropathy
Occasional (5-29%)HP:0009830
Palpebronasal fold
Occasional (5-29%)HP:0000286
Persistent blue colour of hands or feet
Occasional (5-29%)HP:0001063
Redundant neck skin
Occasional (5-29%)HP:0005989
Respiratory insufficiency
Occasional (5-29%)HP:0002093
Round facies
Occasional (5-29%)HP:0000311
Short palpebral fissure
Occasional (5-29%)HP:0012745
Syndactyly
Occasional (5-29%)HP:0001159
Trouble sleeping
Occasional (5-29%)HP:0002360
Uvula bifida
Occasional (5-29%)HP:0000193
Quick Facts
- SNOMED CT
- 26609002
- UMLS CUI
- C1510479
- Fully Specified Name
- Neuralgic amyotrophy (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.