G71.038
BillableOther limb girdle muscular dystrophy
Other limb girdle muscular dystrophy
Coding Notes
Inclusion Terms
Alternative clinical terms for this condition
- LGMD R9 FKRP-related
- LGMD R22 collagen 6-related
- Limb girdle muscular dystrophy due to fukutin related protein dysfunction
- Limb girdle muscular dystrophy type 2I
- Other autosomal recessive limb girdle muscular dystrophy
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
- Limb-girdle muscular dystrophy240046001
- Muscular dystrophy with predominantly proximal limb girdle distribution240046001
- X-linked muscular dystrophy with limb girdle distribution240047005
- X-linked limb girdle muscular dystrophy with normal dystrophin240051007
- Autosomal recessive muscular dystrophy with limb girdle distribution240054004
- X-linked muscular dystrophy not predominantly limb girdle240071003
- Alpha-sarcoglycanopathy LGMD2D (limb girdle muscular dystrophy type 2D)715340002
- Autosomal recessive limb girdle muscular dystrophy type 2D715340002
- Autosomal recessive limb girdle muscular dystrophy type 2A715341003
- Calpain-3 deficiency limb girdle muscular dystrophy type 2A715341003
- Leyden-Möbius muscular dystrophy715341003
- Primary calpainopathy715341003
- Autosomal recessive limb girdle muscular dystrophy type 2C718176005
- Limb girdle muscular dystrophy due to gamma-sarcoglycan deficiency718176005
- Autosomal recessive limb girdle muscular dystrophy type 2F718177001
- Limb girdle muscular dystrophy due to delta-sarcoglycan deficiency718177001
- Autosomal recessive limb girdle muscular dystrophy type 2B718179003
- Limb girdle muscular dystrophy due to dysferlin deficiency718179003
- Autosomal recessive limb girdle muscular dystrophy type 2I718180000
- Limb girdle muscular dystrophy due to deficiency of fukutin related protein718180000
- Autosomal recessive limb girdle muscular dystrophy type 2E718850008
- Limb girdle muscular dystrophy due to beta-sarcoglycan deficiency718850008
- Autosomal recessive limb girdle muscular dystrophy type 2G720522001
- Limb girdle muscular dystrophy due to telethonin deficiency720522001
- Autosomal recessive limb girdle muscular dystrophy type 2K720523006
- Limb girdle muscular dystrophy with intellectual disability syndrome720523006
- Autosomal recessive limb girdle muscular dystrophy type 2J725042001
- Limb-girdle muscular dystrophy 2J titin gene mutation725042001
- Autosomal recessive limb girdle muscular dystrophy type 2O725043006
- Limb-girdle muscular dystrophy 2O POMGNT1 (protein o-mannose beta-1,2-n-acetylglucosaminyltransferase) gene mutation725043006
- Limb-girdle muscular dystrophy 2O POMGNT1 gene mutation725043006
- Autosomal recessive limb girdle muscular dystrophy type 2Y725907002
- Autosomal recessive muscular dystrophy due to LAP1B (lamin-associated protein 1B) deficiency725907002
- Autosomal recessive muscular dystrophy due to Torsin-1A-interacting protein 1 deficiency725907002
- Muscular dystrophy with progressive weakness, distal contracture and rigid spine725907002
- Autosomal recessive limb girdle muscular dystrophy type 2P726614009
- Autosomal recessive limb girdle muscular dystrophy type 2Q726615005
- Autosomal recessive limb girdle muscular dystrophy type 2L726616006
- Autosomal recessive limb girdle muscular dystrophy type 2N726617002
- Autosomal recessive limb girdle muscular dystrophy type 2M726618007
- Autosomal recessive limb girdle muscular dystrophy type 2S732929002
- Autosomal recessive limb girdle muscular dystrophy type 2T732930007
- Autosomal recessive limb girdle muscular dystrophy due to ISPD deficiency783554002
- Autosomal recessive limb girdle muscular dystrophy type 2U783554002
- LGMD2U - autosomal recessive limb girdle muscular dystrophy type 2U783554002
- Autosomal recessive limb girdle muscular dystrophy, cardiac arrhythmia syndrome1179295004
- BVES (blood vessel epicardial substance) related limb girdle muscular dystrophy1179295004
- BVES-related limb girdle muscular dystrophy1179295004
- Blood vessel epicardial substance related limb girdle muscular dystrophy1179295004
- Limb girdle muscular dystrophy 2X1179295004
- Autosomal recessive limb girdle muscular dystrophy type 2W1179297007
- LIM zinc finger domain containing 2-related limb girdle muscular dystrophy1179297007
- LIMS2-related limb girdle muscular dystrophy1179297007
- Limb girdle muscular dystrophy type 2W1179297007
- Childhood-onset progressive contractures, limb girdle weakness, muscle dystrophy syndrome1187251009
- Limb girdle muscular dystrophy due to POMK deficiency1234819007
- Limb girdle muscular dystrophy due to protein O-mannose kinase deficiency1234819007
- Laminin alpha-2 related limb girdle muscular dystrophy R231279883006
- Laminin subunit alpha 2-related LGMD (limb girdle muscular dystrophy) R231279883006
- Laminin subunit alpha 2-related late-onset muscular dystrophy1279883006
- Laminin subunit alpha 2-related limb girdle muscular dystrophy R231279883006
- Limb girdle muscular dystrophy type R241279884000
- POMGNT2-related limb girdle muscular dystrophy R241279884000
- POMGNT2-related muscular dystrophy1279884000
- Protein O-mannose beta-1,4-n-acetylglucosaminyltransferase 2-related limb girdle muscular dystrophy R241279884000
Frequently Asked Questions
What is the ICD-10 code for other limb girdle muscular dystrophy?
The ICD-10-CM code for other limb girdle muscular dystrophy is G71.038. The full clinical description is "Other limb girdle muscular dystrophy". G71.038 is a billable/specific code that can be used on insurance claims and medical billing.
What does ICD-10 code G71.038 mean?
ICD-10-CM code G71.038 represents "Other 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 G71.038 a billable code?
Yes, G71.038 is a billable/specific ICD-10-CM code and can be used to indicate a diagnosis on a medical claim.
What chapter is G71.038 in?
G71.038 is in Chapter 6: Diseases of the Nervous System (codes G00-G99).
What SNOMED CT codes does G71.038 map to?
G71.038 maps to 31 SNOMED CT concepts: 715340002, 783554002, 715341003, 718179003, 718176005, and 26 more. SNOMED CT is a clinical terminology used in electronic health records.
What are the UMLS CUIs for G71.038?
G71.038 is linked to 3 UMLS Concept Unique Identifiers: C5676463, C5676465, C0410161. 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.