G71.220
BillableX-linked myotubular myopathy
X-linked myotubular myopathy
Coding Notes
Inclusion Terms
Alternative clinical terms for this condition
- Myotubular (centronuclear) myopathy
Excludes 2
Conditions not included here, but the patient may have both
- •certain conditions originating in the perinatal periodP04-P96
- •certain infectious and parasitic diseasesA00-B99
- •complications of pregnancy, childbirth and the puerperiumO9A)O00
- •congenital malformations, deformations, and chromosomal abnormalitiesQ00-Q99
- •endocrine, nutritional and metabolic diseasesE00-E88
- •injury, poisoning and certain other consequences of external causesS00-T88
- •neoplasmsC00-D49
- •symptoms, signs and abnormal clinical and laboratory findings, not elsewhere classifiedR00-R94
- •arthrogryposis multiplex congenitaQ74.3
- •metabolic disordersE70-E88
- •myositisM60
Related Codes(1)
Also Known As / Clinical Terms(76)
SNOMED CT
- Myotubular myopathy with type I atrophy15080006
- Severe X-linked myotubular myopathy46804001
- X-linked centronuclear myopathy46804001
- Centronuclear myopathy82077006
- Myotubular myopathy82077006
- X-linked myotubular myopathy, abnormal genitalia syndrome1255278004
- Xq28 contiguous gene deletion syndrome1255278004
- Symptomatic form of X-linked centronuclear myopathy in female carrier1351274008
- Symptomatic form of X-linked myotubular myopathy in female carrier1351274008
UMLS
- CNMXC0410203
- Centronuclear Myopathies, X-LinkedC0410203
- Centronuclear Myopathy, X-LinkedC0410203
- MTMC0410203
- MTM1C0410203
- MTMXC0410203
- MYOPATHY, CENTRONUCLEAR, X-LINKEDC0410203
- MYOTUBULAR MYOPATHY 1C0410203
- MYOTUBULAR MYOPATHY, X-LINKEDC0410203
- Myopathies, X-Linked CentronuclearC0410203
- Myopathies, X-Linked MyotubularC0410203
- Myopathy, X-Linked CentronuclearC0410203
- Myopathy, X-Linked MyotubularC0410203
- Myotubular Myopathies, X-LinkedC0410203
- Myotubular Myopathy 1C0410203
- Myotubular Myopathy, X LinkedC0410203
- Myotubular Myopathy, X-LinkedC0410203
- Severe X-linked myotubular myopathyC0410203
- Severe X-linked myotubular myopathy (disorder)C0410203
- X Linked Centronuclear MyopathyC0410203
- X Linked Myotubular MyopathyC0410203
- X-Linked Centronuclear MyopathiesC0410203
- X-Linked Centronuclear MyopathyC0410203
- X-Linked Myotubular MyopathiesC0410203
- X-Linked Myotubular MyopathyC0410203
- X-linked centronuclear myopathyC0410203
- X-linked myotubular myopathyC0410203
- XLCNMC0410203
- XLMTMC0410203
- XMTMC0410203
- myopathy myotubular x linkC0410203
- x-linked myotubular myopathyC0410203
- Myotubular (centronuclear) myopathyC2875316
Clinical Terms
- X-Linked Myotubular Myopathies
- Severe X-linked myotubular myopathy
- MTM1
- Myopathies, X-Linked Centronuclear
- X-Linked Centronuclear Myopathies
- X-Linked Centronuclear Myopathy
- Centronuclear myopathy
- XLMTM
- XMTM
- Centronuclear Myopathies, X-Linked
- CNMX
- Symptomatic form of X-linked myotubular myopathy in female carrier
- XLCNM
- Symptomatic form of X-linked centronuclear myopathy in female carrier
- Myotubular (centronuclear) myopathy
- Myopathy, X-Linked Centronuclear
- Myotubular myopathy
- X Linked Myotubular Myopathy
- MTM
- MTMX
- MYOTUBULAR MYOPATHY 1
- X-linked myotubular myopathy, abnormal genitalia syndrome
- MYOPATHY, CENTRONUCLEAR, X-LINKED
- Severe X-linked myotubular myopathy (disorder)
- Myotubular myopathy with type I atrophy
- Myopathies, X-Linked Myotubular
- Xq28 contiguous gene deletion syndrome
- myopathy myotubular x link
- Myotubular Myopathies, X-Linked
- Myotubular Myopathy, X-Linked
- Myopathy, X-Linked Myotubular
- X Linked Centronuclear Myopathy
- Centronuclear Myopathy, X-Linked
- Myotubular Myopathy, X Linked
Frequently Asked Questions
What is the ICD-10 code for x-linked myotubular myopathy?
The ICD-10-CM code for x-linked myotubular myopathy is G71.220. The full clinical description is "X-linked myotubular myopathy". G71.220 is a billable/specific code that can be used on insurance claims and medical billing.
What does ICD-10 code G71.220 mean?
ICD-10-CM code G71.220 represents “X-linked myotubular 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 G71.220 a billable code?
Yes, G71.220 is a billable/specific ICD-10-CM code and can be used to indicate a diagnosis on a medical claim.
What chapter is G71.220 in?
G71.220 is in Chapter 6: Diseases of the Nervous System (codes G00-G99).
What SNOMED CT codes does G71.220 map to?
G71.220 maps to 5 SNOMED CT concepts: 82077006, 15080006, 46804001, 1351274008, 1255278004. SNOMED CT is a clinical terminology used in electronic health records.
What are the UMLS CUIs for G71.220?
G71.220 is linked to 2 UMLS Concept Unique Identifiers: C0410203, C2875316. The UMLS (Unified Medical Language System) integrates multiple biomedical vocabularies maintained by the U.S. National Library of Medicine.
How does G71.220 relate to ICF functioning codes?
ICF (International Classification of Functioning, Disability and Health) codes describe how conditions like x-linked myotubular 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 G71.220?
There is no direct ICD-11 mapping available for G71.220 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.