G71.0349
BillableLimb girdle musc dyst due to other sarcoglycan dysfunction
Limb girdle muscular dystrophy due to other sarcoglycan dysfunction
Coding Notes
Inclusion Terms
Alternative clinical terms for this condition
- Delta sarcoglycanopathy
- Delta-sarcoglycan-related LGMD R6
- Gamma sarcoglycanopathy
- Gamma-sarcoglycan-related LGMD R5
- Limb girdle muscular dystrophy type 2C
- Limb girdle muscular dystrophy type 2F
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(71)
UMLS
- ADHALIN DEFICIENCY, SECONDARYC0410173
- Adhalin deficiency, secondaryC0410173
- DMDAC0410173
- DMDA1C0410173
- DUCHENNE-LIKE MUSCULAR DYSTROPHY, AUTOSOMAL RECESSIVE, TYPE 1C0410173
- Duchenne-like muscular dystrophy, autosomal recessive, type 1C0410173
- Gamma sarcoglycanopathyC0410173
- Gamma-sarcoglycan-related LGMD R5C0410173
- Gamma-sarcoglycanopathyC0410173
- LGMD2CC0410173
- LGMDR5C0410173
- Limb girdle muscular dystrophy type 2CC0410173
- Limb-girdle muscular dystrophy with gamma-sarcoglycan deficiencyC0410173
- Limb-girdle muscular dystrophy, type 2CC0410173
- MAGHREBIAN MYOPATHYC0410173
- MUSCULAR DYSTROPHY, DUCHENNE-LIKEC0410173
- MUSCULAR DYSTROPHY, LIMB-GIRDLE, AUTOSOMAL RECESSIVE 5C0410173
- MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 2CC0410173
- Maghrebian myopathyC0410173
- Muscular Dystrophy, Limb-Girdle, Type 2CC0410173
- Muscular dystrophy, Duchenne-likeC0410173
- SARCOGLYCAN, GAMMA, DEFICIENCY OFC0410173
- SCARMDC0410173
- SEVERE CHILDHOOD AUTOSOMAL RECESSIVE MUSCULAR DYSTROPHY, NORTH AFRICAN TYPEC0410173
- Severe childhood autosomal recessive muscular dystrophy, North African typeC0410173
- Autosomal recessive limb girdle muscular dystrophy type 2FC1832525
- Autosomal recessive limb girdle muscular dystrophy type 2F (disorder)C1832525
- Delta-sarcoglycan-related LGMD R6C1832525
- LGMD2FC1832525
- LGMDR6C1832525
- Limb girdle muscular dystrophy due to delta-sarcoglycan deficiencyC1832525
- Limb girdle muscular dystrophy type 2FC1832525
- Limb-girdle muscular dystrophy type 2FC1832525
- MUSCULAR DYSTROPHY, LIMB-GIRDLE, AUTOSOMAL RECESSIVE 6C1832525
- MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 2FC1832525
- Muscular Dystrophy, Limb-Girdle, Type 2FC1832525
- Muscular dystrophy limb-girdle with delta-sarcoglyan deficiencyC1832525
- Delta sarcoglycanopathyC5676460
- Limb girdle musc dyst due to other sarcoglycan dysfunctionC5675015
- Limb girdle muscular dystrophy due to other sarcoglycan dysfunctionC5675015
Clinical Terms
- Limb girdle muscular dystrophy due to delta-sarcoglycan deficiency
- Limb-girdle muscular dystrophy type 2F
- MAGHREBIAN MYOPATHY
- SCARMD
- DUCHENNE-LIKE MUSCULAR DYSTROPHY, AUTOSOMAL RECESSIVE, TYPE 1
- MUSCULAR DYSTROPHY, DUCHENNE-LIKE
- Autosomal recessive limb girdle muscular dystrophy type 2F
- ADHALIN DEFICIENCY, SECONDARY
- Muscular Dystrophy, Limb-Girdle, Type 2F
- Limb-girdle muscular dystrophy, type 2C
- Limb girdle muscular dystrophy type 2F
- DMDA
- Delta-sarcoglycan-related LGMD R6
- MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 2C
- Muscular dystrophy limb-girdle with delta-sarcoglyan deficiency
- Delta sarcoglycanopathy
- LGMDR5
- MUSCULAR DYSTROPHY, LIMB-GIRDLE, AUTOSOMAL RECESSIVE 5
- Limb girdle muscular dystrophy type 2C
- Limb-girdle muscular dystrophy with gamma-sarcoglycan deficiency
- SEVERE CHILDHOOD AUTOSOMAL RECESSIVE MUSCULAR DYSTROPHY, NORTH AFRICAN TYPE
- LGMD2F
- Gamma-sarcoglycan-related LGMD R5
- SARCOGLYCAN, GAMMA, DEFICIENCY OF
- LGMD2C
- Gamma-sarcoglycanopathy
- MUSCULAR DYSTROPHY, LIMB-GIRDLE, AUTOSOMAL RECESSIVE 6
- Gamma sarcoglycanopathy
- Autosomal recessive limb girdle muscular dystrophy type 2F (disorder)
- DMDA1
- LGMDR6
Frequently Asked Questions
What is the ICD-10 code for limb girdle musc dyst due to other sarcoglycan dysfunction?
The ICD-10-CM code for limb girdle musc dyst due to other sarcoglycan dysfunction is G71.0349. The full clinical description is "Limb girdle muscular dystrophy due to other sarcoglycan dysfunction". G71.0349 is a billable/specific code that can be used on insurance claims and medical billing.
What does ICD-10 code G71.0349 mean?
ICD-10-CM code G71.0349 represents “Limb girdle muscular dystrophy due to other 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 G71.0349 a billable code?
Yes, G71.0349 is a billable/specific ICD-10-CM code and can be used to indicate a diagnosis on a medical claim.
What chapter is G71.0349 in?
G71.0349 is in Chapter 6: Diseases of the Nervous System (codes G00-G99).
What are the UMLS CUIs for G71.0349?
G71.0349 is linked to 4 UMLS Concept Unique Identifiers: C0410173, C1832525, C5676460, C5675015. The UMLS (Unified Medical Language System) integrates multiple biomedical vocabularies maintained by the U.S. National Library of Medicine.
How does G71.0349 relate to ICF functioning codes?
ICF (International Classification of Functioning, Disability and Health) codes describe how conditions like limb girdle musc dyst due to other 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 G71.0349?
There is no direct ICD-11 mapping available for G71.0349 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.