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Becker muscular dystrophy

ICD-10: G71.0ORPHA: 98895

Contents

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

Overview

X-linked recessive inherited disorder characterized by slowly progressive muscle weakness of the legs and pelvis

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 Becker muscular dystrophy, sourced from HPO and Orphanet clinical annotations.

Gait disturbanceMyoglobinuriaElevated circulating creatine kinase concentrationMyalgiaExercise intoleranceDifficulty climbing stairsAbnormal urinary colorMuscle weaknessFallsAbnormality of the lower limbElevated circulating hepatic transaminase concentrationMuscle spasmFatiguePes planusSkeletal muscle atrophyTip-toe gaitCardiomyopathy

Classification & Codes

ICD-10 Code

G71.0

Orphanet Code

ORPHA:98895
Becker muscular dystrophy
ICD-10G71.0
OrphanetORPHA:98895
Treatments0 drug(s)
Symptoms on record17 signs
Statuspublished
Factual Authority
Last Updated3/20/2026
Clinical DataHPO · Orphanet
Drug DataFDA · EMA · CDSCO