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G71.038

Other limb girdle muscular dystrophy

Billable FY2026 2025-10-01 → 2026-09-30
Exclusions 11 never code together
G71code
Excludes2
  • arthrogryposis multiplex congenita (Q74.3)Q74.3
  • metabolic disorders (E70-E88)E70-E88
  • myositis (M60.-)M60.-
G00-G99chapter
Excludes2
  • certain conditions originating in the perinatal period (P04-P96)P04-P96
  • certain infectious and parasitic diseases (A00-B99)A00-B99
  • complications of pregnancy, childbirth and the puerperium (O00-O9A)O00-O9A
  • congenital malformations, deformations, and chromosomal abnormalities (Q00-Q99)Q00-Q99
  • endocrine, nutritional and metabolic diseases (E00-E88)E00-E88
  • injury, poisoning and certain other consequences of external causes (S00-T88)S00-T88
  • neoplasms (C00-D49)C00-D49
  • symptoms, signs and abnormal clinical and laboratory findings, not elsewhere classified (R00-R94)R00-R94

Excludes2 — not included here, but the patient may have both. Code both when documented.

Instructional notes 2
G71.038code
Inclusion terms
  • LGMD R22 collagen 6-relatedR22
  • Other autosomal recessive limb girdle muscular dystrophy
Index entries leading here 1
  • Dystrophy, dystrophia
    • muscular G71.00
      • limb-girdle G71.039
        • collagen VI related
        • autosomal recessive NEC G71.038
        • R7 (autosomal recessive) G71.038
        • R8 (autosomal recessive) G71.038
        • R10 (autosomal recessive) G71.038
        • R11 (autosomal recessive) G71.038
        • R13 (autosomal recessive) G71.038
        • R14 (autosomal recessive) G71.038
        • R15 (autosomal recessive) G71.038
        • R16 (autosomal recessive) G71.038
        • R17 (autosomal recessive) G71.038
        • R18 (autosomal recessive) G71.038
        • R19 (autosomal recessive) G71.038
        • R20 (autosomal recessive) G71.038
        • R21 (autosomal recessive) G71.038
        • R22 (autosomal recessive) G71.038
        • R23 (autosomal recessive) G71.038
        • R24 (autosomal recessive) G71.038
        • type 2 (autosomal recessive) G71.038
        • type 2G (autosomal recessive) G71.038
        • type 2H (autosomal recessive) G71.038
        • type 2J (autosomal recessive) G71.038
        • type 2K (autosomal recessive) G71.038
        • type 2M (autosomal recessive) G71.038
        • type 2N (autosomal recessive) G71.038
        • type 2O (autosomal recessive) G71.038
        • type 2P (autosomal recessive) G71.038
        • type 2Q (autosomal recessive) G71.038
        • type 2S (autosomal recessive) G71.038
        • type 2T (autosomal recessive) G71.038
        • type 2U (autosomal recessive) G71.038
        • FKRP-related autosomal recessive G71.038
    • Leyden-Möbius G71.039
      • meaning Limb girdle muscular dystrophy, specified type NEC G71.038
Alongside this code 7 same parent — G71.03
G71.031 Autosomal dominant limb girdle muscular dystrophy G71.032 Autosom recess limb girdle musc dyst d/t calpain-3 dysfnct G71.033 Limb girdle muscular dystrophy due to dysferlin dysfunction G71.034 Limb girdle musc dyst due to sarcoglycan dysfunction category G71.035 Limb girdle musc dyst due to anoctamin-5 dysfunction G71.036 Limb girdle musc dyst due to fukutin related protein dysfnct G71.039 Limb girdle muscular dystrophy, unspecified
Medications 1
10 Muscular Dystrophy, Duchenne drugs

MED-RT files conditions by MeSH, which carves the world differently from ICD-10. These are name matches on this code's description, offered as candidates — not as an assertion that they are this code.

Additional references
AHA Coding Clinic® Licence required

Official coding advice for this code. Published by the American Hospital Association. Not included in this installation.

Risk adjustment

CMS22HCC76 CMS28HCC197 ESRD21HCC76 ESRD24HCC76

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This code

Billable
yes
Code set
FY2026
Parent
G71.03
Block
G70-G73
Siblings
7

Present FY2024–FY2027.