ICD-10-CM Diagnosis Code G71.02
Effective Date: 10/01/2018 To 09/30/2025Facioscapulohumeral muscular dystrophy
| CMS-HCC-V24 | CMS-HCC-V28 | RxHCC | Age | Gender | Maternity | Acute or Chronic | MCC |
|---|---|---|---|---|---|---|---|
| 76 | 197 | -- | -- | -- | -- | Chronic | No |
Applicable To for G71.02:
Back-references to G71.02
Atrophy, atrophic(of)
Disease, diseased see also Syndrome
Dystrophy, dystrophia
Erb's
Fascioscapulohumeral myopathy G71.02
Landouzy-Déjérine dystrophy or facioscapulohumeral atrophy G71.02
Myopathy G72.9
Paralysis, paralytic(complete) (incomplete) G83.9
Pseudohypertrophic muscular dystrophy(Erb's) G71.02
Scapulohumeral myopathy G71.02
- Landouzy-Déjérine G71.02
- fascioscapulohumeral(Landouzy- Déjérine) G71.02
- muscle, muscular(diffuse) (general) (idiopathic) (primary) M62.50
- pseudohypertrophic G71.02
- pseudohypertrophic G71.02
- pseudohypertrophic(muscle) G71.02
- Erb(-Landouzy) G71.02
- Erb's G71.02
- Landouzy-Déjérine G71.02
- muscular G71.00
- Erb type G71.02
- Landouzy-Déjérine type G71.02
- facioscapulohumeral G71.02
- scapulohumeral G71.02
- Erb type G71.02
- disease G71.02
- pseudohypertrophic muscular dystrophy G71.02
- facioscapulohumeral G71.02
- scapulohumeral G71.02
- muscle, muscular NEC G72.89
- pseudohypertrophic G71.02
- pseudohypertrophic G71.02
Chapter, Section and Diagnosis Prefix for
G71.02