G71.2
Non-billableCongenital myopathies
Congenital myopathies
This is a header/category code. For billing purposes, use a more specific child code from the list below.
Coding Notes
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.-)
Child Codes (4)
Also Known As / Clinical Terms
Frequently Asked Questions
What is ICD-10 code G71.2?
ICD-10-CM code G71.2 represents "Congenital myopathies". It is a non-billable header code — use a more specific child code for billing purposes.
Is G71.2 a billable code?
No, G71.2 is a non-billable header code. You need to use one of its more specific child codes for billing. There are 4 child codes under G71.2.
What chapter is G71.2 in?
G71.2 is in Chapter 6: Diseases of the Nervous System (codes G00-G99).
What are the subcategories under G71.2?
G71.2 has 4 child codes, including: G71.20 (Congenital myopathy, unspecified), G71.21 (Nemaline myopathy), G71.22 (Centronuclear myopathy), G71.29 (Other congenital myopathy).
What are the UMLS CUIs for G71.2?
G71.2 is linked to 1 UMLS Concept Unique Identifier: C0270960. 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.