Hereditary neuralgic amyotrophy
ICD-10: G54.5ORPHA: 2901
Overview
neuralgic disorder
Available Treatments (0)
No treatments linked yet
Clinical trials or compassionate use may be available — consult a specialist.
Clinical Presentation
Signs and symptoms associated with Hereditary neuralgic amyotrophy, sourced from HPO and Orphanet clinical annotations.
PolyneuropathyArthralgiaEMG abnormalityUpper limb muscle weaknessUpper limb amyotrophyUpper limb painSprengel anomalyParesthesiaScapular wingingNarrow mouthCleft palateBifid uvulaEpicanthusRound faceAcrocyanosisSyndactylyRespiratory insufficiencyAbnormal speech patternSleep disturbanceShort statureRedundant neck skinPeripheral neuropathyShort palpebral fissureHypoesthesia
Classification & Codes
ICD-10 Code
G54.5Orphanet Code
ORPHA:2901Hereditary neuralgic amyotrophy
| ICD-10 | G54.5 |
| Orphanet | ORPHA:2901 |
| Treatments | 0 drug(s) |
| Symptoms on record | 24 signs |
| Status | published |
Factual Authority
Last Updated3/20/2026
Clinical DataHPO · Orphanet
Drug DataFDA · EMA · CDSCO