G71.035
Limb girdle muscular dystrophy due to anoctamin-5 dysfunction
Billable FY2026 2025-10-01 → 2026-09-30
Exclusions 11 never code together
G71code
G00-G99chapter
Excludes2
- certain conditions originating in the perinatal period (P04-P96)P04-P96
- certain infectious and parasitic diseases (A00-B99)A00-B99
- complications of pregnancy, childbirth and the puerperium (O00-O9A)O00-O9A
- congenital malformations, deformations, and chromosomal abnormalities (Q00-Q99)Q00-Q99
- endocrine, nutritional and metabolic diseases (E00-E88)E00-E88
- injury, poisoning and certain other consequences of external causes (S00-T88)S00-T88
- neoplasms (C00-D49)C00-D49
- symptoms, signs and abnormal clinical and laboratory findings, not elsewhere classified (R00-R94)R00-R94
Excludes2 — not included here, but the patient may have both. Code both when documented.
Instructional notes 4
Index entries leading here 3
Alongside this code 7 same parent — G71.03
G71.031 Autosomal dominant limb girdle muscular dystrophy G71.032 Autosom recess limb girdle musc dyst d/t calpain-3 dysfnct G71.033 Limb girdle muscular dystrophy due to dysferlin dysfunction G71.034 Limb girdle musc dyst due to sarcoglycan dysfunction category G71.036 Limb girdle musc dyst due to fukutin related protein dysfnct G71.038 Other limb girdle muscular dystrophy G71.039 Limb girdle muscular dystrophy, unspecified
Medications 1
MED-RT files conditions by MeSH, which carves the world differently from ICD-10. These are name matches on this code's description, offered as candidates — not as an assertion that they are this code.
Additional references
AHA Coding Clinic® Licence required
Official coding advice for this code. Published by the American Hospital Association. Not included in this installation.