OrphanDrug
OrphanDrug
Pharma Knowledge Base

tibial hemimelia

ICD-10: Q72.5MeSH: C535563ORPHA: 93322

Contents

  1. 1. Overview
  2. 2. Available Treatments
  3. 3. Clinical Presentation
  4. 4. Classification & Codes

Overview

Tibial hemimelia is a rare congenital anomaly characterized by deficiency of the tibia with a relatively intact 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 tibial hemimelia, sourced from HPO and Orphanet clinical annotations.

Talipes equinovarusAbsent tibiaSplit handMesomelic leg shorteningKnee flexion contractureSyndactylyHip dysplasiaSplit footMetatarsus adductusFoot oligodactylyAbsent radiusRadial ray deficiencyShort tibiaProximal tibial and fibular fusionRudimentary to absent tibiaeAnkle hypermobilityTarsal synostosisAplasia of the 2nd metacarpalAplasia of the 4th metacarpalPolydactylyCutaneous finger syndactylyOligodactylyAbsent halluxPartial absence of footCryptorchidismHypospadiasAmbiguous genitaliaCleft palateHearing impairmentMyelomeningoceleCoxa valgaHip dislocationHemivertebrae

Classification & Codes

ICD-10 Code

Q72.5

MeSH Code

C535563

Orphanet Code

ORPHA:93322
tibial hemimelia
ICD-10Q72.5
MeSHC535563
OrphanetORPHA:93322
Treatments0 drug(s)
Symptoms on record33 signs
Statuspublished
Factual Authority
Last Updated3/20/2026
Clinical DataHPO · Orphanet
Drug DataFDA · EMA · CDSCO