G71.035
BillableLimb girdle musc dyst due to anoctamin-5 dysfunction
Limb girdle muscular dystrophy due to anoctamin-5 dysfunction
Coding Notes
Inclusion Terms
Alternative clinical terms for this condition
- •Anoctamin-5-related LGMDR12
- Anoctaminopathy
- Autosomal recessive limb girdle muscular dystrophy type 2L
- Miyoshi myopathy type 3
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
G71.033Limb girdle muscular dystrophy due to dysferlin dysfunction
G71.034Limb girdle musc dyst due to sarcoglycan dysfunction
G71.038Other limb girdle muscular dystrophy
G71.039Limb girdle muscular dystrophy, unspecified
Also Known As / Clinical Terms(21)
UMLS
- Anoctamin-5-related LGMD R12C1969785
- Autosomal recessive limb girdle muscular dystrophy type 2LC1969785
- Autosomal recessive limb girdle muscular dystrophy type 2L (disorder)C1969785
- LGMD2LC1969785
- LGMDR12C1969785
- MUSCULAR DYSTROPHY, LIMB-GIRDLE, AUTOSOMAL RECESSIVE 12C1969785
- MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 2LC1969785
- Muscular Dystrophy, Limb-Girdle, Type 2LC1969785
- AnoctaminopathyC5676461
- Limb girdle musc dyst due to anoctamin-5 dysfunctionC5675016
- Limb girdle muscular dystrophy due to anoctamin-5 dysfunctionC5675016
- Miyoshi myopathy type 3C5676462
Clinical Terms
- Anoctamin-5-related LGMD R12
- LGMD2L
- MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 2L
- Miyoshi myopathy type 3
- LGMDR12
- MUSCULAR DYSTROPHY, LIMB-GIRDLE, AUTOSOMAL RECESSIVE 12
- Anoctaminopathy
- Autosomal recessive limb girdle muscular dystrophy type 2L
- Autosomal recessive limb girdle muscular dystrophy type 2L (disorder)
Frequently Asked Questions
What is the ICD-10 code for limb girdle musc dyst due to anoctamin-5 dysfunction?
The ICD-10-CM code for limb girdle musc dyst due to anoctamin-5 dysfunction is G71.035. The full clinical description is "Limb girdle muscular dystrophy due to anoctamin-5 dysfunction". G71.035 is a billable/specific code that can be used on insurance claims and medical billing.
What does ICD-10 code G71.035 mean?
ICD-10-CM code G71.035 represents “Limb girdle muscular dystrophy due to anoctamin-5 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 G71.035 a billable code?
Yes, G71.035 is a billable/specific ICD-10-CM code and can be used to indicate a diagnosis on a medical claim.
What chapter is G71.035 in?
G71.035 is in Chapter 6: Diseases of the Nervous System (codes G00-G99).
What are the UMLS CUIs for G71.035?
G71.035 is linked to 4 UMLS Concept Unique Identifiers: C1969785, C5676461, C5675016, C5676462. The UMLS (Unified Medical Language System) integrates multiple biomedical vocabularies maintained by the U.S. National Library of Medicine.
How does G71.035 relate to ICF functioning codes?
ICF (International Classification of Functioning, Disability and Health) codes describe how conditions like limb girdle musc dyst due to anoctamin-5 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 G71.035?
There is no direct ICD-11 mapping available for G71.035 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.