Facioscapulohumeral muscular dystrophy
Billable / specificHCC V28 197
G71.02 is a billable, specific ICD-10-CM code that can be used to indicate a diagnosis for reimbursement purposes in FY2027.
Inclusion terms
Applicable to
- Scapulohumeral muscular dystrophy
Excludes2
Not included here — may be reported together when both conditions exist.
- certain conditions originating in the perinatal period (P04-P96) (from G71)
- certain infectious and parasitic diseases (A00-B99) (from G71)
- complications of pregnancy, childbirth and the puerperium (O00-O9A) (from G71)
- congenital malformations, deformations, and chromosomal abnormalities (Q00-Q99) (from G71)
- endocrine, nutritional and metabolic diseases (E00-E88) (from G71)
- injury, poisoning and certain other consequences of external causes (S00-T88) (from G71)
- neoplasms (C00-D49) (from G71)
- symptoms, signs and abnormal clinical and laboratory findings, not elsewhere classified (R00-R94) (from G71)
- arthrogryposis multiplex congenita (Q74.3) (from G71)
- metabolic disorders (E70-E88) (from G71)
- myositis (M60.-) (from G71)
Also known as
- Scapulohumeral muscular dystrophy
- Atrophy, atrophic, fascioscapulohumeral
- Atrophy, atrophic, Landouzy-Déjérine
- Atrophy, atrophic, muscle, muscular, pseudohypertrophic
- Atrophy, atrophic, pseudohypertrophic
- Disease, diseased, Erb
- Dystrophy, dystrophia, Erb's
- Dystrophy, dystrophia, Landouzy-Déjérine
- Dystrophy, dystrophia, muscular, Erb type
- Dystrophy, dystrophia, muscular, facioscapulohumeral
- Dystrophy, dystrophia, muscular, Landouzy-Déjérine type
- Dystrophy, dystrophia, muscular, scapulohumeral
- Erb's, disease
- Erb's, pseudohypertrophic muscular dystrophy
- Fascioscapulohumeral myopathy
- Landouzy-Déjérine dystrophy or facioscapulohumeral atrophy
Parent code
- G71.0Muscular dystrophyHeader