G71.03
Limb girdle muscular dystrophies
Header / non-billable
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G71.03 needs more characters to be billable. Pick the specific code below.
- 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 dysfunctionMore levels
- 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
- G71.039Limb girdle muscular dystrophy, unspecifiedBillable
This code does not map to a risk-adjusting HCC in the loaded models.
Coding notes
Excludes 1 never coded together · Excludes 2 may co-exist
Inherited from G71Primary disorders of muscles
Inherited from chapter 6Diseases of the nervous system
Excludes 2
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)