E88.42
BillableMERRF syndrome
MERRF syndrome
Coding Notes
Inclusion Terms
Alternative clinical terms for this condition
- Myoclonic epilepsy associated with ragged-red fibers
Excludes 1
Codes that cannot be used together with this code (mutual exclusion)
- transitory endocrine and metabolic disorders specific to newborn (P70-P74)
- androgen insensitivity syndrome (E34.5-)
- congenital adrenal hyperplasia (E25.0)
- hemolytic anemias attributable to enzyme disorders (D55.-)
- Marfan syndrome (Q87.4-)
- 5-alpha-reductase deficiency (E29.1)
- histiocytosis X (chronic) (C96.6)
- disorders of pyruvate metabolism (E74.4)
- Kearns-Sayre syndrome (H49.81)
- Leber's disease (H47.22)
- Leigh's encephalopathy (G31.82)
- Mitochondrial myopathy, NEC (G71.3)
- Reye's syndrome (G93.7)
Excludes 2
Conditions not included here, but the patient may have both
- Ehlers-Danlos syndromes (Q79.6-)
Use Additional Code
Additional codes that should follow this code
- codes for associated conditions
Code Also
A second code may be required; sequencing depends on circumstances
- progressive myoclonic epilepsy (G40.3-)
Also Known As / Clinical Terms
SNOMED CT
UMLS
- FUKUHARA DISC0162672
- Fukuhara DiseaseC0162672
- Fukuhara SyndromeC0162672
- Fukuhara diseaseC0162672
- Fukuhara syndromeC0162672
- MERRFC0162672
- MERRF - myoclonic epilepsy with ragged red fibersC0162672
- MERRF - myoclonic epilepsy with ragged red fibresC0162672
- MERRF SYNDROMEC0162672
- MERRF SyndromeC0162672
- MERRF syndromeC0162672
- MYOCLONIC EPILEPSY ASSOCIATED WITH RAGGED-RED FIBERSC0162672
- Myoclonic Epilepsy Associated with Ragged Red FibersC0162672
- Myoclonic Epilepsy Associated with Ragged-Red FibersC0162672
- Myoclonic Epilepsy and Ragged Red FibersC0162672
- Myoclonic Epilepsy with Ragged Red FibersC0162672
- Myoclonic Epilepsy with Ragged-Red FibersC0162672
- Myoclonic epilepsy and ragged-red fibersC0162672
- Myoclonic epilepsy and ragged-red fibresC0162672
- Myoclonic epilepsy associated with ragged-red fibersC0162672
- Myoclonic epilepsy with ragged red fibersC0162672
- Myoclonic epilepsy with ragged red fibers (disorder)C0162672
- Myoclonic epilepsy with ragged red fibresC0162672
- Myoclonic epilepsy with ragged-red fibersC0162672
- Myoclonus with Epilepsy with Ragged Red FibersC0162672
- Myoencephalopathy Ragged Red Fiber DiseaseC0162672
- Myoencephalopathy Ragged-Red Fiber DiseaseC0162672
- Myoencephalopathy ragged-red fiber diseaseC0162672
- Syndrome, FukuharaC0162672
- Syndrome, MERRFC0162672
- epilepsy fiber myoclonic ragged redC0162672
- epilepsy fibers myoclonic ragged redC0162672
- epilepsy fibers myoclonus ragged redC0162672
- epilepsy fibres myoclonic ragged redC0162672
- merrfC0162672
- merrf syndromeC0162672
Frequently Asked Questions
What is the ICD-10 code for merrf syndrome?
The ICD-10-CM code for merrf syndrome is E88.42. The full clinical description is "MERRF syndrome". E88.42 is a billable/specific code that can be used on insurance claims and medical billing.
What does ICD-10 code E88.42 mean?
ICD-10-CM code E88.42 represents "MERRF syndrome". It is classified under Chapter 4: Endocrine, Nutritional and Metabolic Diseases and is a billable/specific code that can be used on a claim.
Is E88.42 a billable code?
Yes, E88.42 is a billable/specific ICD-10-CM code and can be used to indicate a diagnosis on a medical claim.
What chapter is E88.42 in?
E88.42 is in Chapter 4: Endocrine, Nutritional and Metabolic Diseases (codes E00-E89).
What codes cannot be used with E88.42?
E88.42 has Excludes1 notes indicating codes that cannot be used together with it, including: transitory endocrine and metabolic disorders specific to newborn (P70-P74); androgen insensitivity syndrome (E34.5-); congenital adrenal hyperplasia (E25.0); and 10 more.
Are additional codes required with E88.42?
Yes, when using E88.42 you should also code: codes for associated conditions.
What SNOMED CT codes does E88.42 map to?
E88.42 maps to 1 SNOMED CT concept: 230426003. SNOMED CT is a clinical terminology used in electronic health records.
What are the UMLS CUIs for E88.42?
E88.42 is linked to 1 UMLS Concept Unique Identifier: C0162672. 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.