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 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)
- arthrogryposis multiplex congenita (Q74.3)
- metabolic disorders (E70-E88)
- myositis (M60.-)
Also Known As / Clinical Terms
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
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.
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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.