ICD-10-CM Diagnosis Code G71.032
Effective Date: 10/01/2022 To 09/30/2025Autosomal recessive limb girdle muscular dystrophy due to calpain-3 dysfunction
| CMS-HCC-V24 | CMS-HCC-V28 | RxHCC | Age | Gender | Maternity | Acute or Chronic | MCC |
|---|---|---|---|---|---|---|---|
| 76 | 197 | -- | -- | -- | -- | Acute | No |
Applicable To for G71.032:
Back-references to G71.032
Calpainopathy(primary) G71.032
Dystrophy, dystrophia
- autosomal recessive G71.032
- Leyden-Möbius see also Dystrophy, muscular, limb-girdle, by type G71.039
- meaning Limb girdle muscular dystrophy type 2A(autosomal recessive) G71.032
- meaning Limb girdle muscular dystrophy type 2A(autosomal recessive) G71.032
- muscular G71.00
- limb-girdle G71.039
- R1(autosomal recessive) G71.032
- calpain-3-related G71.032
- autosomal recessive G71.032
- autosomal recessive G71.032
- type 2A(autosomal recessive) G71.032
- R1(autosomal recessive) G71.032
- limb-girdle G71.039
Chapter, Section and Diagnosis Prefix for
G71.032