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 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
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
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.
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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.