G71.21
BillableNemaline myopathy
Nemaline myopathy
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.-)
Also Known As / Clinical Terms
SNOMED CT
- Nemaline body disease75072002
- Nemaline myopathy75072002
- Rod myopathy75072002
- Rod-body myopathy75072002
- Congenital nemaline myopathy129621001
- Nemaline myopathy, early onset type129621001
- Adult-onset nemaline myopathy129622008
- Nemaline myopathy, late onset type129622008
- Progressive weakness of muscle1137511009
- Typical nemaline myopathy1197153000
- Childhood-onset nemaline myopathy1197154006
- Mild nemaline myopathy1197154006
- Amish nemaline myopathy1197155007
- Intermediate nemaline myopathy1197156008
- Severe congenital nemaline myopathy1197157004
UMLS
- Myopathies, NemalineC0206157
- Myopathies, RodC0206157
- Myopathies, Rod-BodyC0206157
- Myopathies, nemalineC0206157
- Myopathy, NemalineC0206157
- Myopathy, RodC0206157
- Myopathy, Rod BodyC0206157
- Myopathy, Rod-BodyC0206157
- Myopathy, nemalineC0206157
- Nemaline Body DiseaseC0206157
- Nemaline MyopathiesC0206157
- Nemaline MyopathyC0206157
- Nemaline Rod DiseaseC0206157
- Nemaline body diseaseC0206157
- Nemaline myopathyC0206157
- Nemaline myopathy (disorder)C0206157
- Nemaline rod diseaseC0206157
- Rod Body DiseaseC0206157
- Rod Body MyopathyC0206157
- Rod MyopathiesC0206157
- Rod MyopathyC0206157
- Rod body diseaseC0206157
- Rod myopathyC0206157
- Rod-Body MyopathiesC0206157
- Rod-Body MyopathyC0206157
- Rod-body myopathyC0206157
- nemaline myopathyC0206157
- rod myopathyC0206157
Frequently Asked Questions
What is the ICD-10 code for nemaline myopathy?
The ICD-10-CM code for nemaline myopathy is G71.21. The full clinical description is "Nemaline myopathy". G71.21 is a billable/specific code that can be used on insurance claims and medical billing.
What does ICD-10 code G71.21 mean?
ICD-10-CM code G71.21 represents "Nemaline 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 G71.21 a billable code?
Yes, G71.21 is a billable/specific ICD-10-CM code and can be used to indicate a diagnosis on a medical claim.
What chapter is G71.21 in?
G71.21 is in Chapter 6: Diseases of the Nervous System (codes G00-G99).
What SNOMED CT codes does G71.21 map to?
G71.21 maps to 9 SNOMED CT concepts: 129622008, 1197155007, 1197154006, 129621001, 1197156008, and 4 more. SNOMED CT is a clinical terminology used in electronic health records.
What are the UMLS CUIs for G71.21?
G71.21 is linked to 1 UMLS Concept Unique Identifier: C0206157. 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.