AutoICD API

G71.29

Billable

Other congenital myopathy

Other congenital myopathy

Status

Billable / Specific

Block

G70-G73

Parent Code

G71.2

Coding Notes

Inclusion Terms

Alternative clinical terms for this condition

  • Central core disease
  • Minicore disease
  • Multicore disease
  • Multiminicore disease

Excludes 2

Conditions not included here, but the patient may have both

Related Codes(3)
G71.20

Congenital myopathy, unspecified

BillableG71.21

Nemaline myopathy

BillableG71.22

Centronuclear myopathy

Also Known As / Clinical Terms(336)

SNOMED CT

UMLS

Clinical Terms

  • Autosomal dominant congenital fibre-type disproportion myopathy due to selenoprotein N mutation
  • Congenital fiber-type disproportion myopathy due to ACTA1 mutation
  • Congenital generalized hypercontractile muscle stiffness syndrome
  • Rod-body myopathy
  • Antenatal multi-minicore disease with arthrogryposis multiplex congenita
  • Minicore disease
  • MULTIMINICORE DISEASE WITH EXTERNAL OPHTHALMOPLEGIA
  • Multiminicore Disease
  • Congenital myopathy with fast-twitch fibre atrophy
  • Central Core Diseases
  • Shy-Magee Syndrome
  • central core myopathy
  • Autosomal recessive congenital fiber-type disproportion myopathy due to tropomyosin 3 mutation
  • Congenital fiber-type disproportion myopathy due to ZAK mutation
  • Congenital myopathy with fiber type disproportion
  • Congenital myopathy with caps
  • EMARDD (early-onset myopathy, areflexia, respiratory distress, dysphagia) syndrome
  • Myopathy with cytoplasmic inclusions
  • Autosomal recessive congenital fibre-type disproportion myopathy due to tropomyosin 3 mutation
  • Congenital myopathy with reduced type II muscle fibres
  • Congenital fiber-type disproportion myopathy due to myosin heavy chain 7 mutation
  • Congenital myopathy with type II fibre atrophy
  • Primrose syndrome
  • Autosomal dominant congenital fibre-type disproportion myopathy due to tropomyosin 3 mutation
  • Autosomal recessive congenital fiber-type disproportion myopathy due to ACTA1 mutation
  • Syndrome, Shy-Magee
  • Autosomal dominant central core myopathy
  • Chudley Rozdilsky syndrome
  • Congenital fiber-type disproportion myopathy due to MYH7 mutation
  • Congenital myopathy with internal nuclei and atypical cores
  • Intellectual disability, myopathy, short stature, endocrine defect syndrome
  • Multicore Disease
  • Congenital fibre-type disproportion myopathy due to tropomyosin 3 mutation
  • Intellectual disability, cataract, calcified pinna, myopathy syndrome
  • Cap disease
  • Congenital fibre-type disproportion myopathy due to selenoprotein N mutation
  • Myopathy with type I hypotrophy
  • Akinesia
  • Congenital myosclerosis Lowenthal type
  • Multi-core disease
  • Autosomal dominant congenital fiber-type disproportion myopathy due to selenoprotein N mutation
  • Hyaline body myopathy
  • Nemaline myopathy, early onset type
  • Proximal myopathy
  • Multi-core congenital myopathy (disorder)
  • Congenital myopathy with excess thin filaments
  • MULTICORE MYOPATHY WITH EXTERNAL OPHTHALMOPLEGIA
  • Carey Fineman Ziter syndrome
  • MINICORE MYOPATHY WITH EXTERNAL OPHTHALMOPLEGIA
  • CMYO1B
  • Early-onset myopathy, areflexia, respiratory distress, dysphagia syndrome
  • MINICORE MYOPATHY
  • Pagetoid amyotrophic lateral sclerosis
  • Early onset desmin related myopathy
  • Autosomal recessive congenital fibre-type disproportion myopathy due to actin alpha 1, skeletal muscle mutation
  • Congenital fibre-type disproportion myopathy due to TPM3 mutation
  • Congenital lethal myopathy Compton North type
  • Congenital fiber-type disproportion myopathy due to actin alpha 1, skeletal muscle mutation
  • Autosomal dominant congenital fiber-type disproportion myopathy due to tropomyosin 3 mutation
  • Autosomal dominant congenital fibre-type disproportion myopathy due to SELENON mutation
  • Congenital fiber-type disproportion myopathy due to tropomyosin 3 mutation
  • MULTICORE MYOPATHY
  • Multi-minicore disease
  • Congenital fiber-type disproportion myopathy due to SELENON mutation
  • Congenital fibre-type disproportion myopathy due to SELENON mutation
  • Myosclerosis
  • Autosomal recessive congenital fibre-type disproportion myopathy due to ACTA1 mutation
  • Zebra body myopathy
  • Autosomal dominant congenital fiber-type disproportion myopathy due to ACTA1 mutation
  • Centronuclear myopathy type 4
  • Myopathy with abnormality of histochemical fibre type
  • Myosin storage myopathy
  • Congenital fibre-type disproportion myopathy due to MYH7 mutation
  • Myopathy with tubular aggregates
  • Congenital multi-minicore disease with external ophthalmoplegia
  • Congenital myopathy with fibre type disproportion
  • Congenital myopathy with uniform fiber type
  • Autosomal recessive congenital fiber-type disproportion myopathy due to selenoprotein N mutation
  • Multiminicore myopathy
  • Congenital nonprogressive myopathy with Moebius and Robin sequences
  • Congenital myopathy with myasthenic-like onset
  • Desmin related myopathy with Mallory body-like inclusions
  • Rod myopathy
  • Myopathy with hexagonally cross-linked tubular arrays
  • Autosomal dominant congenital fibre-type disproportion myopathy due to actin alpha 1, skeletal muscle mutation
  • Nemaline myopathy 3
  • Myopathy with abnormality of histochemical fiber type
  • Autosomal dominant congenital fiber-type disproportion myopathy due to actin alpha 1, skeletal muscle mutation
  • CNM6 - centronuclear myopathy 6
  • Autosomal recessive congenital fiber-type disproportion myopathy due to actin alpha 1, skeletal muscle mutation
  • Central core disease (disorder)
  • Bethlem myopathy
  • Autosomal recessive central core disease
  • Actin accumulation myopathy
  • Central Core Disease
  • Congenital fibre-type disproportion myopathy due to ZAK mutation
  • Nemaline body disease
  • Pagetoid neuroskeletal syndrome
  • Congenital myopathy with type 2 muscle fibre atrophy
  • Benign autosomal dominant myopathy
  • Inclusion body myopathy with early-onset Paget disease and frontotemporal dementia
  • Central Core Myopathies
  • Autosomal dominant congenital fiber-type disproportion myopathy due to SELENON mutation
  • Congenital myopathy with fast-twitch fiber atrophy
  • Congenital fibre-type disproportion myopathy due to ACTA1 mutation
  • Congenital myopathy with reduced type 2 muscle fibers
  • Congenital myopathy with type II fiber atrophy
  • Autosomal dominant central core disease
  • Congenital myopathy with type 2 muscle fiber atrophy
  • CENTRAL CORE DIS
  • Congenital generalised hypercontractile muscle stiffness syndrome
  • Autosomal recessive congenital fibre-type disproportion myopathy due to TPM3 mutation
  • Autosomal dominant congenital fibre-type disproportion myopathy due to ACTA1 mutation
  • MmD
  • Muscular dystrophy limb-girdle with Paget disease of bone
  • Nemaline myopathy
  • Congenital myopathy with reduced type II muscle fibers
  • Autosomal recessive congenital fibre-type disproportion myopathy due to selenoprotein N mutation
  • Myopathy, Central Core
  • Autosomal recessive congenital fiber-type disproportion myopathy due to SELENON mutation
  • Autosomal recessive congenital fiber-type disproportion myopathy due to TPM3 mutation
  • Shy Magee Syndrome
  • Calcification of pinna
  • Congenital nemaline myopathy
  • Reducing-body myopathy
  • Shy's disease
  • Congenital fibre-type disproportion myopathy due to actin alpha 1, skeletal muscle mutation
  • Benign congenital myopathy
  • Autosomal dominant congenital fibre-type disproportion myopathy due to TPM3 mutation
  • Autosomal dominant congenital fiber-type disproportion myopathy due to TPM3 mutation
  • Desmin-related myofibrillar myopathy
  • Autosomal recessive congenital fibre-type disproportion myopathy due to SELENON mutation
  • Central Core Disease of Muscle
  • Cap myopathy
  • Congenital fiber-type disproportion myopathy due to selenoprotein N mutation
  • Cylindrical spirals myopathy
  • Sarcotubular myopathy
  • Myopathies, Central Core
  • Congenital myopathy with uniform fibre type
  • Congenital myopathy with abnormal subcellular organelles
  • Congenital fibre-type disproportion myopathy due to myosin heavy chain 7 mutation
  • Lower motor neuron degeneration with Paget-like bone disease
  • CONGENITAL MYOPATHY 1B, AUTOSOMAL RECESSIVE
  • CCO
  • Pinnal calcification
  • Autosomal recessive central core myopathy
  • Muscle filaminopathy
  • IBMPFD - Inclusion body myopathy with early onset Paget disease and frontotemporal dementia
  • Congenital myopathy with reduced type 2 muscle fibres
  • Multi-core congenital myopathy
  • CCD
  • Benign Samaritan congenital myopathy
  • Congenital fiber-type disproportion myopathy due to TPM3 mutation
  • Desminopathy
Frequently Asked Questions
What is the ICD-10 code for other congenital myopathy?

The ICD-10-CM code for other congenital myopathy is G71.29. The full clinical description is "Other congenital myopathy". G71.29 is a billable/specific code that can be used on insurance claims and medical billing.

What does ICD-10 code G71.29 mean?

ICD-10-CM code G71.29 represents “Other congenital myopathy”. 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 G71.29 a billable code?

Yes, G71.29 is a billable/specific ICD-10-CM code and can be used to indicate a diagnosis on a medical claim.

What chapter is G71.29 in?

G71.29 is in Chapter 6: Diseases of the Nervous System (codes G00-G99).

What SNOMED CT codes does G71.29 map to?

G71.29 maps to 54 SNOMED CT concepts: 702349003, 33994004, 1259119003, 1201861004, 1208415001, and 49 more. SNOMED CT is a clinical terminology used in electronic health records.

What are the UMLS CUIs for G71.29?

G71.29 is linked to 4 UMLS Concept Unique Identifiers: C0751951, C1850674, C0270962, C5384690. The UMLS (Unified Medical Language System) integrates multiple biomedical vocabularies maintained by the U.S. National Library of Medicine.

How does G71.29 relate to ICF functioning codes?

ICF (International Classification of Functioning, Disability and Health) codes describe how conditions like other congenital myopathy 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 G71.29?

There is no direct ICD-11 mapping available for G71.29 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.