G71.031 – Autosomal dominant limb girdle muscular dystrophy
ICD-10-CM 2027 diagnosis code · Diseases of myoneural junction and muscle
ICD-10-CM code
G71.031
- Code
G71.031(claims format:G71031)- Description
- Autosomal dominant limb girdle muscular dystrophy
- Billable
- Yes – valid for HIPAA-covered transactions
- Valid for
- Dates of service October 1, 2026 – September 30, 2027 (FY2027)
- Chapter
- 6. Diseases of the nervous system (G00-G99)
- Block
- G70-G73 Diseases of myoneural junction and muscle
- Parent codes
- G71 › G71.0 › G71.03
Notes for G71.031
Applicable to:
- LGMD D4 calpain-3-related
- LGMD D5 collagen 6-related
- Limb girdle muscular dystrophy type 1
Notes inherited from parent codes
Instructional notes at a category or block level apply to every code below it.
G71 – Primary disorders of muscles
Index terms for G71.031
Entries in the ICD-10-CM alphabetic index that lead to this code:
- Calpainopathy, autosomal dominant
- Dystrophy, dystrophia, muscular, limb-girdle, D1
- Dystrophy, dystrophia, muscular, limb-girdle, D2
- Dystrophy, dystrophia, muscular, limb-girdle, D3
- Dystrophy, dystrophia, muscular, limb-girdle, D4
- Dystrophy, dystrophia, muscular, limb-girdle, D5
- Dystrophy, dystrophia, muscular, limb-girdle, type 1
- Dystrophy, dystrophia, muscular, limb-girdle, type 1A
- Dystrophy, dystrophia, muscular, limb-girdle, type 1B
- Dystrophy, dystrophia, muscular, limb-girdle, type 1C
- Dystrophy, dystrophia, muscular, limb-girdle, type 1E
- Dystrophy, dystrophia, muscular, limb-girdle, type 1H
- Dystrophy, dystrophia, muscular, limb-girdle, type 1I
- Dystrophy, dystrophia, muscular, limb-girdle, calpain-3-related, autosomal dominant
- Dystrophy, dystrophia, muscular, limb-girdle, collagen VI related, autosomal dominant
Related codes in G71.03
- G71.032 – Autosomal recessive limb girdle muscular dystrophy due to calpain-3 dysfunctionBillable
- G71.033 – Limb girdle muscular dystrophy due to dysferlin dysfunctionBillable
- G71.034 – Limb girdle muscular dystrophy due to sarcoglycan dysfunctionHeader
- G71.035 – Limb girdle muscular dystrophy due to anoctamin-5 dysfunctionBillable
- G71.036 – Limb girdle muscular dystrophy due to fukutin related protein dysfunctionBillable
- G71.038 – Other limb girdle muscular dystrophyBillable
- G71.039 – Limb girdle muscular dystrophy, unspecifiedBillable
Frequently asked questions
What is ICD-10 code G71.031?
G71.031 is the ICD-10-CM code for autosomal dominant limb girdle muscular dystrophy, in the block G70-G73 (Diseases of myoneural junction and muscle).
Is G71.031 a billable code?
Yes. G71.031 is a billable/specific code that can be used to indicate a diagnosis for reimbursement purposes.
What category does G71.031 belong to?
It belongs to category G71 – Primary disorders of muscles.
Source: CDC/NCHS ICD-10-CM FY2027 code files, tabular list and index. Reference only – code assignment must follow the official ICD-10-CM guidelines and documentation in the medical record.