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 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
- 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
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.
Automate ICD-10 Coding With AI
Send clinical text to the AutoICD API and get back structured ICD-10 codes with confidence scores. Integrates into any EHR or billing system in minutes.
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.