Diagnosis Code: G71.29

Short Description: Other congenital myopathy

Long Description: Other congenital myopathy

The code G71.29 is VALID for claim submission

Code Classification:

• Diseases of the nervous system (G00–G99)
  • Diseases of myoneural junction and muscle (G70-G73)
    • Primary disorders of muscles (G71)
      • G71.29 Other congenital myopathy

Code Version: 2022 ICD-10-CM

Synonyms

• Actin accumulation myopathy
• Akinesia
• Antenatal multi-minicore disease with arthrogryposis multiplex congenita
• Autosomal dominant central core disease
• Autosomal dominant congenital fiber-type disproportion myopathy due to ACTA1 mutation
• Autosomal dominant congenital fiber-type disproportion myopathy due to SELENON mutation
• Autosomal dominant congenital fiber-type disproportion myopathy due to TPM3 mutation
• Autosomal recessive central core disease
• Autosomal recessive congenital fiber-type disproportion myopathy due to ACTA1 mutation
• Autosomal recessive congenital fiber-type disproportion myopathy due to SELENON mutation
• Autosomal recessive congenital fiber-type disproportion myopathy due to TPM3 mutation
• Benign congenital myopathy
• Benign Samaritan congenital myopathy
• Bethlem myopathy
• Cap myopathy
• Central core disease
• Congenital articular rigidity with myopathy
• Congenital fiber-type disproportion myopathy due to ACTA1 mutation
• Congenital fiber-type disproportion myopathy due to ACTA1 mutation
• Congenital fiber-type disproportion myopathy due to ACTA1 mutation
• Congenital fiber-type disproportion myopathy due to MYH7 mutation
• Congenital fiber-type disproportion myopathy due to SELENON mutation
• Congenital fiber-type disproportion myopathy due to TPM3 mutation
• Congenital fiber-type disproportion myopathy due to ZAK mutation
• Congenital generalized hypercontractile muscle stiffness syndrome
• Congenital lethal myopathy Compton North type
• Congenital multi-minicore disease with external ophthalmoplegia
• Congenital myopathy with abnormal subcellular organelles
• Congenital myopathy with fiber type disproportion
• Congenital myopathy with internal nuclei and atypical cores
• Congenital myopathy with myasthenic-like onset
• Congenital myopathy with reduced type 2 muscle fibers
• Congenital myopathy with uniform fiber type
• Congenital nonprogressive myopathy with Moebius and Robin sequences
• Cylindrical spirals myopathy
• Desmin related myopathy with Mallory body-like inclusions
• Desmin-related myofibrillar myopathy
• Duane anomaly, myopathy, scoliosis syndrome
• Duane's syndrome, type 3
• Early-onset myopathy, areflexia, respiratory distress, dysphagia syndrome
• Inclusion body myopathy with early-onset Paget disease and frontotemporal dementia
• Intellectual disability, cataract, calcified pinna, myopathy syndrome
• Intellectual disability, myopathy, short stature, endocrine defect syndrome
• Multi-core congenital myopathy
• Multi-core congenital myopathy
• Multi-core congenital myopathy
• Muscle filaminopathy
• Myopathy with abnormality of histochemical fiber type
• Myopathy with cytoplasmic inclusions
• Myopathy with cytoplasmic inclusions
• Myopathy with hexagonally cross-linked tubular arrays
• Myopathy with tubular aggregates
• Myopathy with type I hypotrophy
• Myosclerosis
• Myosin storage myopathy
• Nemaline myopathy
• Nemaline myopathy, early onset type
• Pinnal calcification
• Proximal myopathy
• Reducing-body myopathy
• Sarcotubular myopathy
• Zebra body myopathy

References to Index of Diseases and Injuries

The code G71.29 has the following ICD-10-CM references to the Index of Diseases and Injuries

• Inclusion Terms:
  • Central core disease
  • Minicore disease
  • Multicore disease
  • Multiminicore disease

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This page was last updated on: 10/1/2023

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