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 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
UMLS
- LGMD2DC2936332
- LGMDR3C2936332
- 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
- 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
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.
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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.