Limb girdle muscular dystrophy, unspecified
Billable / specificHCC V28 197
G71.039 is a billable, specific ICD-10-CM code that can be used to indicate a diagnosis for reimbursement purposes in FY2027.
Excludes2
Not included here — may be reported together when both conditions exist.
- certain conditions originating in the perinatal period (P04-P96) (from G71)
- certain infectious and parasitic diseases (A00-B99) (from G71)
- complications of pregnancy, childbirth and the puerperium (O00-O9A) (from G71)
- congenital malformations, deformations, and chromosomal abnormalities (Q00-Q99) (from G71)
- endocrine, nutritional and metabolic diseases (E00-E88) (from G71)
- injury, poisoning and certain other consequences of external causes (S00-T88) (from G71)
- neoplasms (C00-D49) (from G71)
- symptoms, signs and abnormal clinical and laboratory findings, not elsewhere classified (R00-R94) (from G71)
- arthrogryposis multiplex congenita (Q74.3) (from G71)
- metabolic disorders (E70-E88) (from G71)
- myositis (M60.-) (from G71)
Also known as
- Dystrophy, dystrophia, Leyden-Möbius
- Dystrophy, dystrophia, Leyden-Möbius, meaning Limb girdle muscular dystrophy NOS
- Dystrophy, dystrophia, muscular, limb-girdle
Parent code
- G71.03Limb girdle muscular dystrophiesHeader
Related codes
- G71.031Autosomal dominant limb girdle muscular dystrophyBillable
- G71.032Autosomal recessive limb girdle muscular dystrophy due to calpain-3 dysfunctionBillable
- G71.033Limb girdle muscular dystrophy due to dysferlin dysfunctionBillable
- G71.034Limb girdle muscular dystrophy due to sarcoglycan dysfunctionHeader
- G71.035Limb girdle muscular dystrophy due to anoctamin-5 dysfunctionBillable
- G71.036Limb girdle muscular dystrophy due to fukutin related protein dysfunctionBillable
- G71.038Other limb girdle muscular dystrophyBillable