G71.038 Other limb girdle muscular dystrophy

Billable ICD-10-CM code, FY2026.

Applicable to

• LGMD R22 collagen 6-related
• Other autosomal recessive limb girdle muscular dystrophy

Applies from G71 Primary disorders of muscles

Excludes2 (not included here)

• arthrogryposis multiplex congenita (Q74.3)
• metabolic disorders (E70-E88)
• myositis (M60.-)

Risk adjustment (HCC)

• CMS-HCC V28: HCC 197 — Muscular Dystrophy
• CMS-HCC V22: HCC 76 — Muscular Dystrophy
• ESRD V24: HCC 76

MS-DRG index

Defines the logic of DRG(s) 091-093 in MDC 01.

Code annotations containing back-references to G71.038

Back-references to G71.0

• Code First: Z99.3 Dependence on wheelchair ("muscular dystrophy (G71.0-)")

Back-references to G71

• Code First: M62.84 Sarcopenia ("primary disorders of muscles (G71.-)")

Diagnosis Index entries for G71.038

• Dystrophy, dystrophia › Leyden-Möbius › meaning Limb girdle muscular dystrophy, specified type NEC
• Dystrophy, dystrophia › muscular › limb-girdle › autosomal recessive NEC
• Dystrophy, dystrophia › muscular › limb-girdle › collagen VI related › autosomal recessive
• Dystrophy, dystrophia › muscular › limb-girdle › FKRP-related autosomal recessive
• Dystrophy, dystrophia › muscular › limb-girdle › R7 (autosomal recessive)
• Dystrophy, dystrophia › muscular › limb-girdle › R8 (autosomal recessive)
• Dystrophy, dystrophia › muscular › limb-girdle › R10 (autosomal recessive)
• Dystrophy, dystrophia › muscular › limb-girdle › R11 (autosomal recessive)
• Dystrophy, dystrophia › muscular › limb-girdle › R13 (autosomal recessive)
• Dystrophy, dystrophia › muscular › limb-girdle › R14 (autosomal recessive)
• Dystrophy, dystrophia › muscular › limb-girdle › R15 (autosomal recessive)
• Dystrophy, dystrophia › muscular › limb-girdle › R16 (autosomal recessive)
• Dystrophy, dystrophia › muscular › limb-girdle › R17 (autosomal recessive)
• Dystrophy, dystrophia › muscular › limb-girdle › R18 (autosomal recessive)
• Dystrophy, dystrophia › muscular › limb-girdle › R19 (autosomal recessive)
• Dystrophy, dystrophia › muscular › limb-girdle › R20 (autosomal recessive)
• Dystrophy, dystrophia › muscular › limb-girdle › R21 (autosomal recessive)
• Dystrophy, dystrophia › muscular › limb-girdle › R22 (autosomal recessive)
• Dystrophy, dystrophia › muscular › limb-girdle › R23 (autosomal recessive)
• Dystrophy, dystrophia › muscular › limb-girdle › R24 (autosomal recessive)
• Dystrophy, dystrophia › muscular › limb-girdle › type 2 (autosomal recessive)
• Dystrophy, dystrophia › muscular › limb-girdle › type 2 (autosomal recessive) › specified NEC
• Dystrophy, dystrophia › muscular › limb-girdle › type 2G (autosomal recessive)
• Dystrophy, dystrophia › muscular › limb-girdle › type 2H (autosomal recessive)
• Dystrophy, dystrophia › muscular › limb-girdle › type 2J (autosomal recessive)
• Dystrophy, dystrophia › muscular › limb-girdle › type 2K (autosomal recessive)
• Dystrophy, dystrophia › muscular › limb-girdle › type 2M (autosomal recessive)
• Dystrophy, dystrophia › muscular › limb-girdle › type 2N (autosomal recessive)
• Dystrophy, dystrophia › muscular › limb-girdle › type 2O (autosomal recessive)
• Dystrophy, dystrophia › muscular › limb-girdle › type 2P (autosomal recessive)
• Dystrophy, dystrophia › muscular › limb-girdle › type 2Q (autosomal recessive)
• Dystrophy, dystrophia › muscular › limb-girdle › type 2S (autosomal recessive)
• Dystrophy, dystrophia › muscular › limb-girdle › type 2T (autosomal recessive)
• Dystrophy, dystrophia › muscular › limb-girdle › type 2U (autosomal recessive)

Nearby codes

• G71.0341 Limb girdle muscular dystrophy due to alpha sarcoglycan dysfunction
• G71.0342 Limb girdle muscular dystrophy due to beta sarcoglycan dysfunction
• G71.0349 Limb girdle muscular dystrophy due to other sarcoglycan dysfunction
• G71.035 Limb girdle muscular dystrophy due to anoctamin-5 dysfunction
• G71.036 Limb girdle muscular dystrophy due to fukutin related protein dysfunction
• G71.038 Other limb girdle muscular dystrophy (this code)
• G71.039 Limb girdle muscular dystrophy, unspecified
• G71.09 Other specified muscular dystrophies
• G71.1 Myotonic disorders
• G71.11 Myotonic muscular dystrophy
• G71.12 Myotonia congenita