G71.02
BillableFacioscapulohumeral muscular dystrophy
Facioscapulohumeral muscular dystrophy
Coding Notes
Inclusion Terms
Alternative clinical terms for this condition
- Scapulohumeral muscular dystrophy
Excludes 2
Conditions not included here, but the patient may have both
- •certain conditions originating in the perinatal periodP04-P96
- •certain infectious and parasitic diseasesA00-B99
- •complications of pregnancy, childbirth and the puerperiumO9A)O00
- •congenital malformations, deformations, and chromosomal abnormalitiesQ00-Q99
- •endocrine, nutritional and metabolic diseasesE00-E88
- •injury, poisoning and certain other consequences of external causesS00-T88
- •neoplasmsC00-D49
- •symptoms, signs and abnormal clinical and laboratory findings, not elsewhere classifiedR00-R94
- •arthrogryposis multiplex congenitaQ74.3
- •metabolic disordersE70-E88
- •myositisM60
Related Codes(4)
Also Known As / Clinical Terms(90)
SNOMED CT
- Autosomal recessive muscular dystrophy not predominantly limb girdle240073000
- Scapulohumeral muscular dystrophy240074006
- Autosomal dominant muscular dystrophy not predominantly limb girdle240075007
- FMD - Facioscapulohumeral muscular dystrophy399091004
- FSH - Facioscapulohumeral muscular dystrophy399091004
- FSHD - Facioscapulohumeral muscular dystrophy399091004
- Facioscapulohumeral muscular dystrophy399091004
- Fascioscapulohumeral muscular dystrophy399091004
- Landouzy-Dejerine muscular dystrophy399091004
- Landouzy-Déjérine muscular dystrophy399091004
UMLS
- Atrophies, FacioscapulohumeralC0238288
- Atrophy, FacioscapulohumeralC0238288
- Dystrophies, Facioscapulohumeral MuscularC0238288
- Dystrophies, Landouzy-DejerineC0238288
- Dystrophy, Facioscapulohumeral MuscularC0238288
- Dystrophy, Landouzy-DejerineC0238288
- FACIOSCAPULOHUMERAL MUSCULAR DYSTROPHYC0238288
- FMDC0238288
- FMD - Facioscapulohumeral muscular dystrophyC0238288
- FSH - Facioscapulohumeral muscular dystrophyC0238288
- FSH Muscular DystrophyC0238288
- FSH muscular dystrophyC0238288
- FSHDC0238288
- FSHD - Facioscapulohumeral muscular dystrophyC0238288
- Facio-Scapulo-Humeral DystrophyC0238288
- Facio-scapulo-humeral dystrophyC0238288
- Facioscapulohumeral AtrophiesC0238288
- Facioscapulohumeral AtrophyC0238288
- Facioscapulohumeral Muscular DystrophiesC0238288
- Facioscapulohumeral Muscular DystrophyC0238288
- Facioscapulohumeral Type Progressive Muscular DystrophyC0238288
- Facioscapulohumeral atrophyC0238288
- Facioscapulohumeral muscular dystrophyC0238288
- Facioscapulohumeral muscular dystrophy (disorder)C0238288
- Facioscapulohumeral type progressive muscular dystrophyC0238288
- Facioscapuloperoneal Muscular DystrophyC0238288
- Facioscapuloperoneal muscular dystrophyC0238288
- Fascioscapulohumeral muscular dystrophyC0238288
- LANDOUZY-DEJERINE MUSCULAR DYSTROPHYC0238288
- Landouzy Dejerine DystrophyC0238288
- Landouzy Dejerine muscular dystrophyC0238288
- Landouzy-Dejerine DystrophiesC0238288
- Landouzy-Dejerine DystrophyC0238288
- Landouzy-Dejerine muscular dystrophyC0238288
- Landouzy-Déjérine muscular dystrophyC0238288
- Muscular Dystrophies, FacioscapulohumeralC0238288
- Muscular Dystrophy, FacioscapulohumeralC0238288
- Muscular Dystrophy, Landouzy DejerineC0238288
- Muscular dystrophy, facioscapulohumeralC0238288
- Progressive Muscular Dystrophy, Facioscapulohumeral TypeC0238288
- facioscapulohumeral muscular dystrophyC0238288
- MUSCULAR DYSTROPHY, SCAPULOHUMERALC0410192
- Muscular Dystrophy, ScapulohumeralC0410192
- Scapulohumeral muscular dystrophyC0410192
- Scapulohumeral muscular dystrophy (disorder)C0410192
Clinical Terms
- Atrophy, Facioscapulohumeral
- Landouzy-Déjérine muscular dystrophy
- FSH muscular dystrophy
- Muscular Dystrophy, Scapulohumeral
- Progressive Muscular Dystrophy, Facioscapulohumeral Type
- Facioscapuloperoneal muscular dystrophy
- Muscular Dystrophies, Facioscapulohumeral
- Muscular dystrophy, facioscapulohumeral
- Landouzy-Dejerine Dystrophy
- Facioscapulohumeral atrophy
- Facio-scapulo-humeral dystrophy
- Facioscapulohumeral Type Progressive Muscular Dystrophy
- Dystrophy, Facioscapulohumeral Muscular
- FSHD
- Landouzy Dejerine muscular dystrophy
- FSH - Facioscapulohumeral muscular dystrophy
- FMD - Facioscapulohumeral muscular dystrophy
- Muscular Dystrophy, Landouzy Dejerine
- Fascioscapulohumeral muscular dystrophy
- Landouzy-Dejerine muscular dystrophy
- Facioscapulohumeral Atrophies
- Atrophies, Facioscapulohumeral
- Scapulohumeral muscular dystrophy (disorder)
- Dystrophy, Landouzy-Dejerine
- Scapulohumeral muscular dystrophy
- Landouzy Dejerine Dystrophy
- Autosomal dominant muscular dystrophy not predominantly limb girdle
- Facioscapulohumeral Muscular Dystrophies
- FMD
- Dystrophies, Landouzy-Dejerine
- Autosomal recessive muscular dystrophy not predominantly limb girdle
- Facioscapulohumeral muscular dystrophy (disorder)
- Landouzy-Dejerine Dystrophies
- FSHD - Facioscapulohumeral muscular dystrophy
- Dystrophies, Facioscapulohumeral Muscular
Frequently Asked Questions
What is the ICD-10 code for facioscapulohumeral muscular dystrophy?
The ICD-10-CM code for facioscapulohumeral muscular dystrophy is G71.02. The full clinical description is "Facioscapulohumeral muscular dystrophy". G71.02 is a billable/specific code that can be used on insurance claims and medical billing.
What does ICD-10 code G71.02 mean?
ICD-10-CM code G71.02 represents “Facioscapulohumeral muscular dystrophy”. It is classified under Chapter 6: Diseases of the Nervous System and is a billable/specific code that can be used on a claim.
Is G71.02 a billable code?
Yes, G71.02 is a billable/specific ICD-10-CM code and can be used to indicate a diagnosis on a medical claim.
What chapter is G71.02 in?
G71.02 is in Chapter 6: Diseases of the Nervous System (codes G00-G99).
What SNOMED CT codes does G71.02 map to?
G71.02 maps to 4 SNOMED CT concepts: 240075007, 240073000, 399091004, 240074006. SNOMED CT is a clinical terminology used in electronic health records.
What are the UMLS CUIs for G71.02?
G71.02 is linked to 2 UMLS Concept Unique Identifiers: C0238288, C0410192. The UMLS (Unified Medical Language System) integrates multiple biomedical vocabularies maintained by the U.S. National Library of Medicine.
How does G71.02 relate to ICF functioning codes?
ICF (International Classification of Functioning, Disability and Health) codes describe how conditions like facioscapulohumeral muscular dystrophy affect a person's functioning — body functions, activities, participation, and environmental factors. AutoICD provides ICF Core Sets for 12+ conditions and can map clinical text to ICF categories automatically. Browse the ICF directory to explore functioning codes.
What is the ICD-11 equivalent of G71.02?
There is no direct ICD-11 mapping available for G71.02 in the WHO crosswalk tables. This may mean the concept is classified differently in ICD-11. Use the ICD-10 to ICD-11 converter to search for related codes.
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Includes SNOMED Clinical Terms® (SNOMED CT®) used by permission of SNOMED International. Includes content from the UMLS Metathesaurus, courtesy of the U.S. National Library of Medicine.