- G71.038 is a billable/specific ICD-10-CM code that can be used to indicate a diagnosis for reimbursement purposes.
- The 2024 edition of ICD-10-CM G71.038 became effective on October 1, 2022.
- This is the American ICD-10-CM version of G71.038 – other international versions of ICD-10 G71.038 may differ.
ICD-10-CM G71.038 is grouped within Diagnostic Related Group(s):
- 091 Other disorders of nervous system with mcc
- 092 Other disorders of nervous system with cc
- 093 Other disorders of nervous system without cc/mcc
Applicable To
- LGMD R9 FKRP-related
- LGMD R22 collagen 6-related
- Limb girdle muscular dystrophy due to fukutin related protein dysfunction
- Limb girdle muscular dystrophy type 2I
- Other autosomal recessive limb girdle muscular dystrophy
Code History
- 2024 (effective 10/1/2022): New code
- 2024 (effective 10/1/2022): No change
Diagnosis Index entries containing back-references to G71.038:
- meaning Limb girdle muscular dystrophy, specified type NEC > Leyden-Möbius G71.039
- autosomal recessive NEC > limb-girdle G71.039
- autosomal recessive > collagen VI related G71.031
- fukutin related protein dysfunction > due to G71.0341
- FKRP-related autosomal recessive > limb-girdle G71.039
- R7 (autosomal recessive) > limb-girdle G71.039
- R8 (autosomal recessive) > limb-girdle G71.039
- R9 (autosomal recessive) > limb-girdle G71.039
- R10 (autosomal recessive) > limb-girdle G71.039
- R11 (autosomal recessive) > limb-girdle G71.039
- R13 (autosomal recessive) > limb-girdle G71.039
- R14 (autosomal recessive) > limb-girdle G71.039
- R15 (autosomal recessive) > limb-girdle G71.039
- R16 (autosomal recessive) > limb-girdle G71.039
- R17 (autosomal recessive) > limb-girdle G71.039
- R18 (autosomal recessive) > limb-girdle G71.039
- R19 (autosomal recessive) > limb-girdle G71.039
- R20 (autosomal recessive) > limb-girdle G71.039
- R21 (autosomal recessive) > limb-girdle G71.039
- R22 (autosomal recessive) > limb-girdle G71.039
- R23 (autosomal recessive) > limb-girdle G71.039
- R24 (autosomal recessive) > limb-girdle G71.039
- type 2 (autosomal recessive) > limb-girdle G71.039
- specified NEC > type 2 (autosomal recessive) G71.038
- type 2I (autosomal recessive) > limb-girdle G71.039