- G71.031 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 G71.031 became effective on October 1, 2022.
- This is the American ICD-10-CM version of G71.031 – other international versions of ICD-10 G71.031 may differ.
ICD-10-CM G71.031 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 D4 calpain-3-related
- LGMD D5 collagen 6-related
- Limb girdle muscular dystrophy type 1
Code History
- 2024 (effective 10/1/2022): New code
- 2024 (effective 10/1/2022): No change
Diagnosis Index entries containing back-references to G71.031:
- autosomal dominant > Calpainopathy (primary) G71.032
- autosomal dominant > calpain-3-related G71.032
- collagen VI related > limb-girdle G71.039
- autosomal dominant > collagen VI related G71.031
- D1 (autosomal dominant) > limb-girdle G71.039
- D2 (autosomal dominant) > limb-girdle G71.039
- D3 (autosomal dominant) > limb-girdle G71.039
- D4 (autosomal dominant) > limb-girdle G71.039
- D5 (autosomal dominant) > limb-girdle G71.039
- type 1 (autosomal dominant) > limb-girdle G71.039
- type 1A (autosomal dominant) > limb-girdle G71.039
- type 1B (autosomal dominant) > limb-girdle G71.039
- type 1C (autosomal dominant) > limb-girdle G71.039
- type 1E (autosomal dominant) > limb-girdle G71.039
- type 1H (autosomal dominant) > limb-girdle G71.039
- type 1I (autosomal dominant) > limb-girdle G71.039