G71.033
BillableLimb girdle muscular dystrophy due to dysferlin dysfunction
Limb girdle muscular dystrophy due to dysferlin dysfunction
Coding Notes
Inclusion Terms
Alternative clinical terms for this condition
- Dysferlinopathy
- LGMD R2 dysferlin-related
- Limb girdle muscular dystrophy type 2B
- Miyoshi Myopathy type 1
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(6)
G71.031Autosomal dominant limb girdle muscular dystrophy
G71.032Autosom recess limb girdle musc dyst d/t calpain-3 dysfnct
G71.034Limb girdle musc dyst due to sarcoglycan dysfunction
G71.035Limb girdle musc dyst due to anoctamin-5 dysfunction
G71.038Other limb girdle muscular dystrophy
G71.039Limb girdle muscular dystrophy, unspecified
Also Known As / Clinical Terms(35)
UMLS
- Autosomal Recessive Muscular Dystrophy Limb-Girdle 2C1850889
- Autosomal recessive limb girdle muscular dystrophy type 2BC1850889
- Autosomal recessive limb girdle muscular dystrophy type 2B (disorder)C1850889
- LGMD R2 dysferlin-relatedC1850889
- LGMD2BC1850889
- LGMD3C1850889
- LGMDR2C1850889
- Limb girdle muscular dystrophy due to dysferlin deficiencyC1850889
- Limb girdle muscular dystrophy type 2BC1850889
- Limb-Girdle Muscular Dystrophy Type 2BC1850889
- Limb-girdle muscular dystrophy, type 2BC1850889
- MUSCULAR DYSTROPHY, LIMB-GIRDLE, AUTOSOMAL RECESSIVE 2C1850889
- MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 2BC1850889
- MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 3C1850889
- Muscular Dystrophy, Limb-Girdle, Type 2BC1850889
- Muscular dystrophy, limb-girdle, type 3C1850889
- DysferlinopathyC2931687
- Limb girdle muscular dystrophy due to dysferlin dysfunctionC5675011
- Miyoshi Myopathy type 1C5676459
Clinical Terms
- LGMDR2
- LGMD R2 dysferlin-related
- Miyoshi Myopathy type 1
- Muscular Dystrophy, Limb-Girdle, Type 2B
- LGMD2B
- Limb girdle muscular dystrophy due to dysferlin deficiency
- Dysferlinopathy
- MUSCULAR DYSTROPHY, LIMB-GIRDLE, AUTOSOMAL RECESSIVE 2
- Autosomal recessive limb girdle muscular dystrophy type 2B
- Autosomal Recessive Muscular Dystrophy Limb-Girdle 2
- MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 3
- Limb-Girdle Muscular Dystrophy Type 2B
- Limb girdle muscular dystrophy type 2B
- Limb-girdle muscular dystrophy, type 2B
- Autosomal recessive limb girdle muscular dystrophy type 2B (disorder)
- LGMD3
Frequently Asked Questions
What is the ICD-10 code for limb girdle muscular dystrophy due to dysferlin dysfunction?
The ICD-10-CM code for limb girdle muscular dystrophy due to dysferlin dysfunction is G71.033. The full clinical description is "Limb girdle muscular dystrophy due to dysferlin dysfunction". G71.033 is a billable/specific code that can be used on insurance claims and medical billing.
What does ICD-10 code G71.033 mean?
ICD-10-CM code G71.033 represents “Limb girdle muscular dystrophy due to dysferlin dysfunction”. 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 G71.033 a billable code?
Yes, G71.033 is a billable/specific ICD-10-CM code and can be used to indicate a diagnosis on a medical claim.
What chapter is G71.033 in?
G71.033 is in Chapter 6: Diseases of the Nervous System (codes G00-G99).
What are the UMLS CUIs for G71.033?
G71.033 is linked to 4 UMLS Concept Unique Identifiers: C1850889, C2931687, C5675011, C5676459. The UMLS (Unified Medical Language System) integrates multiple biomedical vocabularies maintained by the U.S. National Library of Medicine.
How does G71.033 relate to ICF functioning codes?
ICF (International Classification of Functioning, Disability and Health) codes describe how conditions like limb girdle muscular dystrophy due to dysferlin dysfunction 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 G71.033?
There is no direct ICD-11 mapping available for G71.033 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.