AutoICD API

G71.038

Billable

Other limb girdle muscular dystrophy

Other limb girdle muscular dystrophy

Status

Billable / Specific

Block

G70-G73

Parent Code

G71.03

Coding Notes

Inclusion Terms

Alternative clinical terms for this condition

  • LGMD R9 FKRP-related
  • •LGMD collagen 6-relatedR22
  • 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

Related Codes(6)
G71.031

Autosomal dominant limb girdle muscular dystrophy

BillableG71.032

Autosom recess limb girdle musc dyst d/t calpain-3 dysfnct

BillableG71.033

Limb girdle muscular dystrophy due to dysferlin dysfunction

BillableG71.034

Limb girdle musc dyst due to sarcoglycan dysfunction

G71.035

Limb girdle musc dyst due to anoctamin-5 dysfunction

BillableG71.039

Limb girdle muscular dystrophy, unspecified

Billable
Also Known As / Clinical Terms(135)

SNOMED CT

UMLS

Clinical Terms

  • Limb girdle muscular dystrophy due to delta-sarcoglycan deficiency
  • LGMD2U - autosomal recessive limb girdle muscular dystrophy type 2U
  • Autosomal recessive limb girdle muscular dystrophy type 2S
  • Limb-girdle muscular dystrophy
  • Autosomal recessive limb girdle muscular dystrophy type 2N
  • Limb girdle muscular dystrophy due to POMK deficiency
  • Muscular dystrophy with progressive weakness, distal contracture and rigid spine
  • Autosomal recessive limb girdle muscular dystrophy type 2D
  • Autosomal recessive limb girdle muscular dystrophy type 2T
  • Muscular dystrophy with predominantly proximal limb girdle distribution
  • Autosomal recessive limb girdle muscular dystrophy type 2G
  • LIM zinc finger domain containing 2-related limb girdle muscular dystrophy
  • Autosomal recessive limb girdle muscular dystrophy type 2F
  • Childhood-onset progressive contractures, limb girdle weakness, muscle dystrophy syndrome
  • Autosomal recessive limb girdle muscular dystrophy type 2J
  • X-linked muscular dystrophy with limb girdle distribution
  • Limb girdle muscular dystrophy due to dysferlin deficiency
  • BVES-related limb girdle muscular dystrophy
  • Alpha-sarcoglycanopathy LGMD2D (limb girdle muscular dystrophy type 2D)
  • Limb girdle muscular dystrophy due to telethonin deficiency
  • POMGNT2-related muscular dystrophy
  • Autosomal recessive limb girdle muscular dystrophy type 2Q
  • Limb girdle muscular dystrophy due to gamma-sarcoglycan deficiency
  • Autosomal recessive limb girdle muscular dystrophy, cardiac arrhythmia syndrome
  • Primary calpainopathy
  • Autosomal recessive limb girdle muscular dystrophy type 2A
  • Autosomal recessive limb girdle muscular dystrophy due to ISPD deficiency
  • Autosomal recessive limb girdle muscular dystrophy type 2U
  • Leyden-Möbius muscular dystrophy
  • Laminin subunit alpha 2-related LGMD (limb girdle muscular dystrophy) R23
  • Limb girdle muscular dystrophy type R24
  • Limb-girdle muscular dystrophy 2J titin gene mutation
  • X-linked limb girdle muscular dystrophy with normal dystrophin
  • X-linked muscular dystrophy not predominantly limb girdle
  • Autosomal recessive limb girdle muscular dystrophy type 2E
  • Autosomal recessive limb girdle muscular dystrophy type 2W
  • Limb girdle muscular dystrophy due to beta-sarcoglycan deficiency
  • Autosomal recessive limb girdle muscular dystrophy type 2Y
  • Autosomal recessive muscular dystrophy with limb girdle distribution
  • Autosomal recessive limb girdle muscular dystrophy type 2P
  • Autosomal recessive limb girdle muscular dystrophy type 2B
  • Laminin alpha-2 related limb girdle muscular dystrophy R23
  • Limb girdle muscular dystrophy due to deficiency of fukutin related protein
  • Calpain-3 deficiency limb girdle muscular dystrophy type 2A
  • Autosomal recessive limb girdle muscular dystrophy type 2M
  • Autosomal recessive limb girdle muscular dystrophy type 2O
  • Protein O-mannose beta-1,4-n-acetylglucosaminyltransferase 2-related limb girdle muscular dystrophy R24
  • POMGNT2-related limb girdle muscular dystrophy R24
  • Autosomal recessive limb girdle muscular dystrophy type 2C
  • LIMS2-related limb girdle muscular dystrophy
  • Limb girdle muscular dystrophy 2X
  • Laminin subunit alpha 2-related limb girdle muscular dystrophy R23
  • Autosomal recessive limb girdle muscular dystrophy type 2I
  • Limb girdle muscular dystrophy type 2W
  • Autosomal recessive limb girdle muscular dystrophy type 2K
  • Other autosomal recessive limb girdle muscular dystrophy
  • LGMD R22 collagen 6-related
  • Limb girdle muscular dystrophy due to protein O-mannose kinase deficiency
  • Autosomal recessive muscular dystrophy due to LAP1B (lamin-associated protein 1B) deficiency
  • Laminin subunit alpha 2-related late-onset muscular dystrophy
  • Limb-girdle muscular dystrophy 2O POMGNT1 gene mutation
  • Autosomal recessive muscular dystrophy due to Torsin-1A-interacting protein 1 deficiency
  • Limb girdle muscular dystrophy with intellectual disability syndrome
  • BVES (blood vessel epicardial substance) related limb girdle muscular dystrophy
  • Limb-girdle muscular dystrophy 2O POMGNT1 (protein o-mannose beta-1,2-n-acetylglucosaminyltransferase) gene mutation
  • Autosomal recessive limb girdle muscular dystrophy type 2L
  • Blood vessel epicardial substance related limb girdle muscular dystrophy
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.

How does G71.038 relate to ICF functioning codes?

ICF (International Classification of Functioning, Disability and Health) codes describe how conditions like other 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 G71.038?

There is no direct ICD-11 mapping available for G71.038 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.