G71.031
BillableAutosomal dominant limb girdle muscular dystrophy
Autosomal dominant limb girdle muscular dystrophy
Coding Notes
Inclusion Terms
Alternative clinical terms for this condition
- LGMD D4 calpain-3-related
- LGMD D5 collagen 6-related
- Limb girdle muscular dystrophy type 1
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(6)
G71.032Autosom recess limb girdle musc dyst d/t calpain-3 dysfnct
G71.033Limb girdle muscular dystrophy due to dysferlin dysfunction
G71.034Limb girdle musc dyst due to sarcoglycan dysfunction
G71.035Limb girdle musc dyst due to anoctamin-5 dysfunction
G71.038Other limb girdle muscular dystrophy
G71.039Limb girdle muscular dystrophy, unspecified
Also Known As / Clinical Terms(27)
SNOMED CT
- Autosomal dominant muscular dystrophy with limb girdle distribution240067001
- Autosomal dominant limb girdle muscular dystrophy type 1D719987009
- Autosomal dominant limb girdle muscular dystrophy type 1E719988004
- Autosomal dominant limb girdle muscular dystrophy type 1F719989007
- Autosomal dominant limb girdle muscular dystrophy type 1G719990003
- Autosomal dominant limb-girdle muscular dystrophy type 1H771334000
- Calpain-3-related limb girdle muscular dystrophy D41279886003
- Limb girdle muscular dystrophy type D41279886003
UMLS
Clinical Terms
- LGMD D4 calpain-3-related
- LGMD D5 collagen 6-related
- LGMDD1
- Autosomal dominant limb girdle muscular dystrophy type 1D
- Autosomal dominant limb girdle muscular dystrophy type 1E
- Autosomal dominant limb girdle muscular dystrophy type 1G
- Autosomal dominant muscular dystrophy with limb girdle distribution
- Calpain-3-related limb girdle muscular dystrophy D4
- MUSCULAR DYSTROPHY, LIMB-GIRDLE, AUTOSOMAL DOMINANT 1
- Autosomal dominant limb-girdle muscular dystrophy type 1H
- Limb girdle muscular dystrophy type 1
- Limb girdle muscular dystrophy type D4
- Autosomal dominant limb girdle muscular dystrophy type 1F
Frequently Asked Questions
What is the ICD-10 code for autosomal dominant limb girdle muscular dystrophy?
The ICD-10-CM code for autosomal dominant limb girdle muscular dystrophy is G71.031. The full clinical description is "Autosomal dominant limb girdle muscular dystrophy". G71.031 is a billable/specific code that can be used on insurance claims and medical billing.
What does ICD-10 code G71.031 mean?
ICD-10-CM code G71.031 represents “Autosomal dominant limb girdle muscular dystrophy”. 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 G71.031 a billable code?
Yes, G71.031 is a billable/specific ICD-10-CM code and can be used to indicate a diagnosis on a medical claim.
What chapter is G71.031 in?
G71.031 is in Chapter 6: Diseases of the Nervous System (codes G00-G99).
What SNOMED CT codes does G71.031 map to?
G71.031 maps to 7 SNOMED CT concepts: 719987009, 719988004, 719989007, 719990003, 771334000, and 2 more. SNOMED CT is a clinical terminology used in electronic health records.
What are the UMLS CUIs for G71.031?
G71.031 is linked to 4 UMLS Concept Unique Identifiers: C5675009, C5676457, C5676458, C4721885. The UMLS (Unified Medical Language System) integrates multiple biomedical vocabularies maintained by the U.S. National Library of Medicine.
How does G71.031 relate to ICF functioning codes?
ICF (International Classification of Functioning, Disability and Health) codes describe how conditions like autosomal dominant limb girdle muscular dystrophy 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 G71.031?
There is no direct ICD-11 mapping available for G71.031 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.