fibular hemimelia
ICD-10: Q72.6ORPHA: 93323
Overview
congenital absence of the fibula
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 fibular hemimelia, sourced from HPO and Orphanet clinical annotations.
Joint hypermobilityAbnormal fibula morphologyTalipes equinovarusGenu valgumTibial bowingShort tibiaDisproportionate prominence of the femoral medial condyleLimb undergrowthLower limb asymmetryLimitation of joint mobilityJoint stiffnessToe syndactylyTalipes equinovalgusShort toeBowing of the legsFibular hypoplasiaShort femurDecreased hip abductionArthralgia of the hipLimited knee flexion/extensionFinger syndactylyAnkle hypermobilityStructural foot deformityAbnormal bone ossificationOligodactylyPainHip subluxationProximal femoral focal deficiencyImpairment of activities of daily livingKnee joint hypermobilityRenal dysplasiaAbnormality of the eyeAnophthalmiaAbnormal anterior chamber morphologyIntellectual disabilityCraniosynostosisAbnormal heart morphologyFoot oligodactylyThrombocytopeniaSpina bifidaFibular aplasiaHypoplastic acetabulaeAbnormal morphology of ulnaEctrodactylyThoracoabdominal wall defectGait disturbanceAbnormal lower limb bone morphology
Classification & Codes
ICD-10 Code
Q72.6Orphanet Code
ORPHA:93323fibular hemimelia
| ICD-10 | Q72.6 |
| Orphanet | ORPHA:93323 |
| Treatments | 0 drug(s) |
| Symptoms on record | 47 signs |
| Status | published |
Factual Authority
Last Updated3/20/2026
Clinical DataHPO · Orphanet
Drug DataFDA · EMA · CDSCO