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 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
- 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
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.
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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.