G71.032
BillableAutosom recess limb girdle musc dyst d/t calpain-3 dysfnct
Autosomal recessive limb girdle muscular dystrophy due to calpain-3 dysfunction
Coding Notes
Inclusion Terms
Alternative clinical terms for this condition
- Limb girdle muscular dystrophy type 2A
- LGMD R1 calpain-3-related
- Primary calpainopathy
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
G71.033Limb girdle muscular dystrophy due to dysferlin dysfunction
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(46)
UMLS
- Autosom recess limb girdle musc dyst d/t calpain-3 dysfnctC5675010
- Autosomal recessive limb girdle muscular dystrophy due to calpain-3 dysfunctionC5675010
- Autosomal Recessive Muscular Dystrophy Limb-Girdle 1C1869123
- Autosomal recessive limb girdle muscular dystrophy type 2AC1869123
- Autosomal recessive limb girdle muscular dystrophy type 2A (disorder)C1869123
- CALPAINOPATHYC1869123
- Calpain-3 deficiency limb girdle muscular dystrophy type 2AC1869123
- CalpainopathyC1869123
- LEYDEN-MOEBIUS MUSCULAR DYSTROPHYC1869123
- LGMD R1 calpain-3-relatedC1869123
- LGMD2C1869123
- LGMD2AC1869123
- LGMDR1C1869123
- Leyden-Moebius muscular dystrophyC1869123
- Leyden-Möbius muscular dystrophyC1869123
- Limb girdle muscular dystrophy type 2AC1869123
- Limb-Girdle Muscular Dystrophy Type 2AC1869123
- Limb-girdle muscular dystrophy type 2C1869123
- Limb-girdle muscular dystrophy type 2AC1869123
- MUSCULAR DYSTROPHY, LIMB-GIRDLE, AUTOSOMAL RECESSIVE 1C1869123
- MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 2C1869123
- MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 2AC1869123
- MUSCULAR DYSTROPHY, PELVOFEMORALC1869123
- Muscular Dystrophy, Limb-Girdle, Type 2C1869123
- Muscular Dystrophy, Limb-Girdle, Type 2AC1869123
- Muscular dystrophy, pelvofemoralC1869123
- Primary calpainopathyC1869123
Clinical Terms
- CALPAINOPATHY
- MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 2
- Muscular dystrophy, pelvofemoral
- LGMD R1 calpain-3-related
- Primary calpainopathy
- Limb girdle muscular dystrophy type 2A
- Autosomal recessive limb girdle muscular dystrophy type 2A
- Leyden-Möbius muscular dystrophy
- Limb-girdle muscular dystrophy type 2
- Leyden-Moebius muscular dystrophy
- MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 2A
- Calpain-3 deficiency limb girdle muscular dystrophy type 2A
- Limb-Girdle Muscular Dystrophy Type 2A
- LGMD2
- Autosomal recessive limb girdle muscular dystrophy type 2A (disorder)
- MUSCULAR DYSTROPHY, LIMB-GIRDLE, AUTOSOMAL RECESSIVE 1
- Autosomal Recessive Muscular Dystrophy Limb-Girdle 1
- LGMDR1
- LGMD2A
Frequently Asked Questions
What is the ICD-10 code for autosom recess limb girdle musc dyst d/t calpain-3 dysfnct?
The ICD-10-CM code for autosom recess limb girdle musc dyst d/t calpain-3 dysfnct is G71.032. The full clinical description is "Autosomal recessive limb girdle muscular dystrophy due to calpain-3 dysfunction". G71.032 is a billable/specific code that can be used on insurance claims and medical billing.
What does ICD-10 code G71.032 mean?
ICD-10-CM code G71.032 represents “Autosomal recessive limb girdle muscular dystrophy due to calpain-3 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 G71.032 a billable code?
Yes, G71.032 is a billable/specific ICD-10-CM code and can be used to indicate a diagnosis on a medical claim.
What chapter is G71.032 in?
G71.032 is in Chapter 6: Diseases of the Nervous System (codes G00-G99).
What are the UMLS CUIs for G71.032?
G71.032 is linked to 2 UMLS Concept Unique Identifiers: C5675010, C1869123. The UMLS (Unified Medical Language System) integrates multiple biomedical vocabularies maintained by the U.S. National Library of Medicine.
How does G71.032 relate to ICF functioning codes?
ICF (International Classification of Functioning, Disability and Health) codes describe how conditions like autosom recess limb girdle musc dyst d/t calpain-3 dysfnct 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 G71.032?
There is no direct ICD-11 mapping available for G71.032 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.