G71.29
BillableOther congenital myopathy
Other congenital myopathy
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
- 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
- Akinesia33994004
- Zebra body myopathy34513009
- Reducing-body myopathy42779002
- Central core disease43152001
- Central core myopathy43152001
- Sarcotubular myopathy43226001
- Minicore disease55133004
- Multi-core congenital myopathy55133004
- Multi-core disease55133004
- Multi-minicore disease55133004
- Multicore disease55133004
- Multiminicore disease55133004
- Congenital myopathy with abnormal subcellular organelles68186003
- Nemaline body disease75072002
- Nemaline myopathy75072002
- Rod myopathy75072002
- Rod-body myopathy75072002
- Congenital nemaline myopathy129621001
- Nemaline myopathy, early onset type129621001
- Benign congenital myopathy193222002
- Proximal myopathy193255007
- Calcification of pinna232221001
- Pinnal calcification232221001
- Myopathy with abnormality of histochemical fiber type240082006
- Myopathy with abnormality of histochemical fibre type240082006
- Myopathy with type I hypotrophy240083001
- Congenital myopathy with fiber type disproportion240084007
- Congenital myopathy with fibre type disproportion240084007
- Congenital myopathy with uniform fiber type240085008
- Congenital myopathy with uniform fibre type240085008
- Myopathy with cytoplasmic inclusions240086009
- Myopathy with tubular aggregates240087000
- Carey Fineman Ziter syndrome429753001
- Congenital nonprogressive myopathy with Moebius and Robin sequences429753001
- Hyaline body myopathy699267007
- Myosin storage myopathy699267007
- Actin accumulation myopathy702349003
- Congenital myopathy with excess thin filaments702349003
- Nemaline myopathy 3702349003
- Cap disease703532002
- Cap myopathy703532002
- Congenital myopathy with caps703532002
- IBMPFD - Inclusion body myopathy with early onset Paget disease and frontotemporal dementia703544004
- Inclusion body myopathy with early-onset Paget disease and frontotemporal dementia703544004
- Lower motor neuron degeneration with Paget-like bone disease703544004
- Muscular dystrophy limb-girdle with Paget disease of bone703544004
- Pagetoid amyotrophic lateral sclerosis703544004
- Pagetoid neuroskeletal syndrome703544004
- Desmin related myopathy with Mallory body-like inclusions715646003
- Early onset desmin related myopathy715646003
- Benign autosomal dominant myopathy718572004
- Bethlem myopathy718572004
- Intellectual disability, cataract, calcified pinna, myopathy syndrome726709001
- Primrose syndrome726709001
- Congenital myopathy with myasthenic-like onset763315005
- Congenital myosclerosis Lowenthal type763895001
- Myosclerosis763895001
- Cylindrical spirals myopathy764525006
- Centronuclear myopathy type 4764945007
- Congenital myopathy with internal nuclei and atypical cores764945007
- Chudley Rozdilsky syndrome764959000
- Intellectual disability, myopathy, short stature, endocrine defect syndrome764959000
- Muscle filaminopathy764992006
- Myopathy with hexagonally cross-linked tubular arrays764994007
- Desmin-related myofibrillar myopathy770627003
- Desminopathy770627003
- Benign Samaritan congenital myopathy770787005
- Congenital lethal myopathy Compton North type773306002
- Congenital generalised hypercontractile muscle stiffness syndrome1174000008
- Congenital generalized hypercontractile muscle stiffness syndrome1174000008
- Autosomal dominant central core disease1201861004
- Autosomal dominant central core myopathy1201861004
- Autosomal recessive central core disease1201862006
- Autosomal recessive central core myopathy1201862006
- CNM6 - centronuclear myopathy 61201964008
- Congenital fiber-type disproportion myopathy due to ZAK mutation1201964008
- Congenital fibre-type disproportion myopathy due to ZAK mutation1201964008
- Congenital fiber-type disproportion myopathy due to SELENON mutation1202023003
- Congenital fiber-type disproportion myopathy due to selenoprotein N mutation1202023003
- Congenital fibre-type disproportion myopathy due to SELENON mutation1202023003
- Congenital fibre-type disproportion myopathy due to selenoprotein N mutation1202023003
- Autosomal dominant congenital fiber-type disproportion myopathy due to SELENON mutation1202024009
- Autosomal dominant congenital fiber-type disproportion myopathy due to selenoprotein N mutation1202024009
- Autosomal dominant congenital fibre-type disproportion myopathy due to SELENON mutation1202024009
- Autosomal dominant congenital fibre-type disproportion myopathy due to selenoprotein N mutation1202024009
- Autosomal recessive congenital fiber-type disproportion myopathy due to SELENON mutation1202025005
- Autosomal recessive congenital fiber-type disproportion myopathy due to selenoprotein N mutation1202025005
- Autosomal recessive congenital fibre-type disproportion myopathy due to SELENON mutation1202025005
- Autosomal recessive congenital fibre-type disproportion myopathy due to selenoprotein N mutation1202025005
- Congenital fiber-type disproportion myopathy due to ACTA1 mutation1208413008
- Congenital fiber-type disproportion myopathy due to actin alpha 1, skeletal muscle mutation1208413008
- Congenital fibre-type disproportion myopathy due to ACTA1 mutation1208413008
- Congenital fibre-type disproportion myopathy due to actin alpha 1, skeletal muscle mutation1208413008
- Autosomal recessive congenital fiber-type disproportion myopathy due to ACTA1 mutation1208414002
- Autosomal recessive congenital fiber-type disproportion myopathy due to actin alpha 1, skeletal muscle mutation1208414002
- Autosomal recessive congenital fibre-type disproportion myopathy due to ACTA1 mutation1208414002
- Autosomal recessive congenital fibre-type disproportion myopathy due to actin alpha 1, skeletal muscle mutation1208414002
- Autosomal dominant congenital fiber-type disproportion myopathy due to ACTA1 mutation1208415001
- Autosomal dominant congenital fiber-type disproportion myopathy due to actin alpha 1, skeletal muscle mutation1208415001
- Autosomal dominant congenital fibre-type disproportion myopathy due to ACTA1 mutation1208415001
- Autosomal dominant congenital fibre-type disproportion myopathy due to actin alpha 1, skeletal muscle mutation1208415001
- Congenital fiber-type disproportion myopathy due to TPM3 mutation1208416000
- Congenital fiber-type disproportion myopathy due to tropomyosin 3 mutation1208416000
- Congenital fibre-type disproportion myopathy due to TPM3 mutation1208416000
- Congenital fibre-type disproportion myopathy due to tropomyosin 3 mutation1208416000
- Autosomal recessive congenital fiber-type disproportion myopathy due to TPM3 mutation1208417009
- Autosomal recessive congenital fiber-type disproportion myopathy due to tropomyosin 3 mutation1208417009
- Autosomal recessive congenital fibre-type disproportion myopathy due to TPM3 mutation1208417009
- Autosomal recessive congenital fibre-type disproportion myopathy due to tropomyosin 3 mutation1208417009
- Autosomal dominant congenital fiber-type disproportion myopathy due to TPM3 mutation1208418004
- Autosomal dominant congenital fiber-type disproportion myopathy due to tropomyosin 3 mutation1208418004
- Autosomal dominant congenital fibre-type disproportion myopathy due to TPM3 mutation1208418004
- Autosomal dominant congenital fibre-type disproportion myopathy due to tropomyosin 3 mutation1208418004
- Congenital fiber-type disproportion myopathy due to MYH7 mutation1209168005
- Congenital fiber-type disproportion myopathy due to myosin heavy chain 7 mutation1209168005
- Congenital fibre-type disproportion myopathy due to MYH7 mutation1209168005
- Congenital fibre-type disproportion myopathy due to myosin heavy chain 7 mutation1209168005
- EMARDD (early-onset myopathy, areflexia, respiratory distress, dysphagia) syndrome1236844002
- Early-onset myopathy, areflexia, respiratory distress, dysphagia syndrome1236844002
- Congenital myopathy with fast-twitch fiber atrophy1255274002
- Congenital myopathy with fast-twitch fibre atrophy1255274002
- Congenital myopathy with reduced type 2 muscle fibers1255274002
- Congenital myopathy with reduced type 2 muscle fibres1255274002
- Congenital myopathy with reduced type II muscle fibers1255274002
- Congenital myopathy with reduced type II muscle fibres1255274002
- Congenital myopathy with type 2 muscle fiber atrophy1255274002
- Congenital myopathy with type 2 muscle fibre atrophy1255274002
- Congenital myopathy with type II fiber atrophy1255274002
- Congenital myopathy with type II fibre atrophy1255274002
- Antenatal multi-minicore disease with arthrogryposis multiplex congenita1259119003
- Congenital multi-minicore disease with external ophthalmoplegia1259560001
UMLS
- CCDC0751951
- CCOC0751951
- CENTRAL CORE DISC0751951
- Central Core DiseaseC0751951
- Central Core Disease of MuscleC0751951
- Central Core DiseasesC0751951
- Central Core MyopathiesC0751951
- Central Core MyopathyC0751951
- Central core diseaseC0751951
- Central core disease (disorder)C0751951
- Central core myopathyC0751951
- Myopathies, Central CoreC0751951
- Myopathy, Central CoreC0751951
- Myopathy, central coreC0751951
- Shy Magee SyndromeC0751951
- Shy's diseaseC0751951
- Shy-Magee SyndromeC0751951
- Shy-Magee syndromeC0751951
- Syndrome, Shy-MageeC0751951
- central core diseaseC0751951
- central core myopathyC0751951
- CMYO1BC1850674
- CONGENITAL MYOPATHY 1B, AUTOSOMAL RECESSIVEC1850674
- MINICORE MYOPATHYC1850674
- MINICORE MYOPATHY WITH EXTERNAL OPHTHALMOPLEGIAC1850674
- MULTICORE MYOPATHYC1850674
- MULTICORE MYOPATHY WITH EXTERNAL OPHTHALMOPLEGIAC1850674
- MULTIMINICORE DISEASE WITH EXTERNAL OPHTHALMOPLEGIAC1850674
- MULTIMINICORE MYOPATHYC1850674
- Minicore DiseaseC1850674
- Minicore MyopathyC1850674
- Minicore Myopathy with External OphthalmoplegiaC1850674
- Minicore myopathyC1850674
- MmDC1850674
- Multi-Minicore DiseaseC1850674
- Multicore DiseaseC1850674
- Multicore MyopathyC1850674
- Multicore Myopathy With External OphthalmoplegiaC1850674
- Multiminicore DiseaseC1850674
- Multiminicore Disease With External OphthalmoplegiaC1850674
- Multiminicore MyopathyC1850674
- Minicore diseaseC0270962
- Multi-core congenital myopathyC0270962
- Multi-core congenital myopathy (disorder)C0270962
- Multi-core diseaseC0270962
- Multi-minicore diseaseC0270962
- Multicore diseaseC0270962
- Multicore myopathyC0270962
- Multiminicore diseaseC0270962
- Multiminicore myopathyC0270962
- Other congenital myopathyC5384690
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.
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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.