G71.036BillableSave
G71.036 - Limb girdle muscular dystrophy due to fukutin related protein dysfunction
ICD-10-CM Chapter 6: Diseases of the nervous system · G70-G73 Diseases of myoneural junction and muscle (G70-G73) · Subcategory of G71.03 · FY2027
Applicable To
Inclusion terms listed under G71.036 in the ICD-10-CM tabular list.
- LGMD R9 FKRP-related
- Limb girdle muscular dystrophy due to FKRP deficiency
- Limb girdle muscular dystrophy type 2I
Includes, Excludes and Coding Notes
Excludes 2 — Not Included HereFrom G71
Not part of this code; report both codes when the patient has both conditions.
- arthrogryposis multiplex congenita (Q74.3)
- metabolic disorders (E70-E88)
- myositis (M60.-)
Excludes 2 — Not Included HereFrom Chapter G00-G99
Not part of this code; report both codes when the patient has both conditions.
- 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)
Related condition guides
Documentation requirements, coding pitfalls and FAQs for conditions coded with G71.036.
Chapter Information
Other codes in G71.03
Codes at the same level as G71.036
- Autosomal dominant limb girdle muscular dystrophyG71.031
- Autosomal recessive limb girdle muscular dystrophy due to calpain-3 dysfunctionG71.032
- Limb girdle muscular dystrophy due to dysferlin dysfunctionG71.033
- Limb girdle muscular dystrophy due to sarcoglycan dysfunctionG71.034
- Limb girdle muscular dystrophy due to anoctamin-5 dysfunctionG71.035
- Other limb girdle muscular dystrophyG71.038
- Limb girdle muscular dystrophy, unspecifiedG71.039