ICDcodes.org
FY2027

G71.032 — Autosomal recessive limb girdle muscular dystrophy due to calpain-3 dysfunction

Billable

Is G71.032 billable?

Yes — G71.032 is billable for FY2027. G71.032 is a valid, billable ICD-10-CM code at the highest level of specificity in its branch. G71.032 may be submitted for encounters from October 1, 2026 through September 30, 2027.

G71.032 at a glance

CodeG71.032
DescriptionAutosomal recessive limb girdle muscular dystrophy due to calpain-3 dysfunction
BillableYes
Code setICD-10-CM FY2027
Valid for encountersOctober 1, 2026 – September 30, 2027

Which MS-DRGs does G71.032 group to?

G71.032 sits in MDC 01 and helps define the logic of 3 MS-DRGs (version 44, FY2027). Which one a stay actually groups to also depends on procedures and secondary diagnoses.

  • 091Other Disorders of Nervous System with MCCmedical
  • 092Other Disorders of Nervous System with CCmedical
  • 093Other Disorders of Nervous System without CC/MCCmedical

How is G71.032 listed in the Alphabetic Index?

These are the routes through the Alphabetic Index that lead to G71.032. They show the wording a clinician may have documented, which often differs from the Tabular description.

  • Calpainopathy (primary)
  • Calpainopathy › autosomal recessive (primary)
  • Dystrophy, dystrophia › Leyden-Möbius › meaning Limb girdle muscular dystrophy type 2A
  • Dystrophy, dystrophia › muscular › limb-girdle › calpain-3-related
  • Dystrophy, dystrophia › muscular › limb-girdle › R1
  • Dystrophy, dystrophia › muscular › limb-girdle › type 2A
  • Dystrophy, dystrophia › muscular › limb-girdle › calpain-3-related › autosomal recessive

Inclusion terms

Alternative wording in documentation that is classified to G71.032.

  • Limb girdle muscular dystrophy type 2A
  • LGMD R1 calpain-3-related
  • Primary calpainopathy

Excludes2 — not included here — inherited from Chapter 6

The conditions below are not part of G71.032, but a patient may have both at the same time. When documentation supports it, G71.032 and the excluded code may both be reported.

  • certain conditions originating in the perinatal period (P04-P96)
  • certain infectious and parasitic diseases (A00-B99)
  • complications of pregnancy, childbirth and the puerperium (O00-O9A)
  • congenital malformations, deformations, and chromosomal abnormalities (Q00-Q99)
  • endocrine, nutritional and metabolic diseases (E00-E88)
  • injury, poisoning and certain other consequences of external causes (S00-T88)
  • neoplasms (C00-D49)
  • symptoms, signs and abnormal clinical and laboratory findings, not elsewhere classified (R00-R94)

Excludes2 — not included here — inherited from G71

The conditions below are not part of G71.032, but a patient may have both at the same time. When documentation supports it, G71.032 and the excluded code may both be reported.

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

How long has G71.032 existed?

G71.032 first appears in FY2023.

Derived from the official order files for FY2016–FY2026. FY2017 and FY2020 publish no order file, so those years are not covered.

Which conditions are coded to G71.032?

What other codes are in the G71.03 family? (7)