G71.0341
BillableLimb girdle musc dyst due to alpha sarcoglycan dysfunction
Limb girdle muscular dystrophy due to alpha sarcoglycan dysfunction
Coding Notes
Inclusion Terms
Alternative clinical terms for this condition
- Alpha sarcoglycanopathy
- Limb-girdle muscular dystrophy due to alpha-sarcoglycan deficiency
- Limb girdle muscular dystrophy type 2D
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(3)
Also Known As / Clinical Terms(60)
UMLS
- ADHALINOPATHY, PRIMARYC2936332
- AdhalinopathiesC2936332
- Adhalinopathies, PrimaryC2936332
- Adhalinopathy, PrimaryC2936332
- Alpha SarcoglycanopathiesC2936332
- Alpha SarcoglycanopathyC2936332
- Alpha sarcoglycanopathyC2936332
- Alpha-SarcoglycanopathiesC2936332
- Alpha-SarcoglycanopathyC2936332
- Alpha-sarcoglycanopathy LGMD2D (limb girdle muscular dystrophy type 2D)C2936332
- Autosomal Recessive Muscular Dystrophy Limb-Girdle 3C2936332
- Autosomal recessive limb girdle muscular dystrophy type 2DC2936332
- Autosomal recessive limb girdle muscular dystrophy type 2D (disorder)C2936332
- DMDA2C2936332
- DUCHENNE-LIKE AUTOSOMAL RECESSIVE MUSCULAR DYSTROPHY, TYPE 2C2936332
- Duchenne Like Autosomal Recessive Muscular Dystrophy, Type 2C2936332
- Duchenne-Like Autosomal Recessive Muscular Dystrophy, Type 2C2936332
- LGMD2DC2936332
- LGMDR3C2936332
- Limb Girdle Muscular Dystrophy, Type 2DC2936332
- Limb girdle muscular dystrophy type 2DC2936332
- Limb-Girdle Muscular Dystrophy Type 2DC2936332
- Limb-Girdle Muscular Dystrophy, Type 2DC2936332
- Limb-girdle muscular dystrophy due to alpha-sarcoglycan deficiencyC2936332
- MUSCULAR DYSTROPHY, LIMB-GIRDLE, AUTOSOMAL RECESSIVE 3C2936332
- MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 2DC2936332
- Muscular Dystrophy Limb Girdle with Alpha Sarcoglycan DeficiencyC2936332
- Muscular Dystrophy Limb-Girdle with Alpha-Sarcoglycan DeficiencyC2936332
- Muscular Dystrophy, Limb-Girdle, Type 2DC2936332
- Primary AdhalinopathiesC2936332
- Primary AdhalinopathyC2936332
- Limb girdle musc dyst due to alpha sarcoglycan dysfunctionC5675013
- Limb girdle muscular dystrophy due to alpha sarcoglycan dysfunctionC5675013
Clinical Terms
- Primary Adhalinopathy
- Alpha sarcoglycanopathy
- Autosomal recessive limb girdle muscular dystrophy type 2D
- Limb Girdle Muscular Dystrophy, Type 2D
- Alpha-Sarcoglycanopathy
- Alpha-sarcoglycanopathy LGMD2D (limb girdle muscular dystrophy type 2D)
- Duchenne Like Autosomal Recessive Muscular Dystrophy, Type 2
- Limb-girdle muscular dystrophy due to alpha-sarcoglycan deficiency
- Alpha-Sarcoglycanopathies
- Adhalinopathies, Primary
- Muscular Dystrophy Limb Girdle with Alpha Sarcoglycan Deficiency
- Primary Adhalinopathies
- LGMDR3
- Adhalinopathy, Primary
- DUCHENNE-LIKE AUTOSOMAL RECESSIVE MUSCULAR DYSTROPHY, TYPE 2
- Autosomal recessive limb girdle muscular dystrophy type 2D (disorder)
- Limb-Girdle Muscular Dystrophy Type 2D
- MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 2D
- Alpha Sarcoglycanopathies
- LGMD2D
- Limb girdle muscular dystrophy type 2D
- MUSCULAR DYSTROPHY, LIMB-GIRDLE, AUTOSOMAL RECESSIVE 3
- Muscular Dystrophy Limb-Girdle with Alpha-Sarcoglycan Deficiency
- Adhalinopathies
- DMDA2
- Autosomal Recessive Muscular Dystrophy Limb-Girdle 3
- Limb-Girdle Muscular Dystrophy, Type 2D
Frequently Asked Questions
What is the ICD-10 code for limb girdle musc dyst due to alpha sarcoglycan dysfunction?
The ICD-10-CM code for limb girdle musc dyst due to alpha sarcoglycan dysfunction is G71.0341. The full clinical description is "Limb girdle muscular dystrophy due to alpha sarcoglycan dysfunction". G71.0341 is a billable/specific code that can be used on insurance claims and medical billing.
What does ICD-10 code G71.0341 mean?
ICD-10-CM code G71.0341 represents “Limb girdle muscular dystrophy due to alpha sarcoglycan 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 G71.0341 a billable code?
Yes, G71.0341 is a billable/specific ICD-10-CM code and can be used to indicate a diagnosis on a medical claim.
What chapter is G71.0341 in?
G71.0341 is in Chapter 6: Diseases of the Nervous System (codes G00-G99).
What are the UMLS CUIs for G71.0341?
G71.0341 is linked to 2 UMLS Concept Unique Identifiers: C2936332, C5675013. The UMLS (Unified Medical Language System) integrates multiple biomedical vocabularies maintained by the U.S. National Library of Medicine.
How does G71.0341 relate to ICF functioning codes?
ICF (International Classification of Functioning, Disability and Health) codes describe how conditions like limb girdle musc dyst due to alpha sarcoglycan 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 G71.0341?
There is no direct ICD-11 mapping available for G71.0341 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.