familial congenital mirror movements
ORPHA: 238722
Overview
human disease
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 familial congenital mirror movements, sourced from HPO and Orphanet clinical annotations.
Bimanual synkinesiaClumsinessAbnormal corticospinal tract morphologyEasy fatigabilityPoor fine motor coordinationAbnormality of movementAgenesis of corpus callosumSpecific learning disabilityMyalgiaDysgenesis of the hippocampusHypogonadotropic hypogonadismMild intellectual disabilityFused cervical vertebraeCerebral palsy
Classification & Codes
Orphanet Code
ORPHA:238722familial congenital mirror movements
| Orphanet | ORPHA:238722 |
| Treatments | 0 drug(s) |
| Symptoms on record | 14 signs |
| Status | published |
Factual Authority
Last Updated3/20/2026
Clinical DataHPO · Orphanet
Drug DataFDA · EMA · CDSCO