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 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
- 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
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.
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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.