E88.40
BillableMitochondrial metabolism disorder, unspecified
Mitochondrial metabolism disorder, unspecified
Coding Notes
Excludes 1
Codes that cannot be used together with this code (mutual exclusion)
- •transitory endocrine and metabolic disorders specific to newbornP70-P74
- •androgen insensitivity syndromeE34.5
- •congenital adrenal hyperplasiaE25.0
- •hemolytic anemias attributable to enzyme disordersD55
- •Marfan syndromeQ87.4
- •5-alpha-reductase deficiencyE29.1
- •histiocytosis X (chronic)C96.6
- •disorders of pyruvate metabolismE74.4
- •Kearns-Sayre syndromeH49.81
- •Leber's diseaseH47.22
- •Leigh's encephalopathyG31.82
- •Mitochondrial myopathy, NECG71.3
- •Reye's syndromeG93.7
Use Additional Code
Additional codes that should follow this code
- codes for associated conditions
Related Codes(4)
Also Known As / Clinical Terms(45)
SNOMED CT
- Mitochondrial cytopathy240096000
- Mitochondrial disease240096000
- Hypertrophic mitochondrial cardiomyopathy472316006
- Demyelination of central nervous system co-occurrent and due to mitochondrial disease724784006
- Demyelination of central nervous system with mitochondrial disorder724784006
- Liver disease co-occurrent and due to mitochondrial disorder735732003
- Liver disease with mitochondrial disorder735732003
- Combined oxidative phosphorylation defect type 16771513008
- Infantile hypertrophic cardiomyopathy due to MRPL44 deficiency771513008
- Infantile hypertrophic cardiomyopathy due to mitochondrial ribosomal protein L44 deficiency771513008
- Dilated cardiomyopathy due to mitochondrial disease871639003
- Disorder of glomerulus due to mitochondrial cytopathy1148867008
- Glomerular disease due to mitochondrial cytopathy1148867008
- Non-syndromic mitochondrial sensorineural deafness1187512003
- Chorea due to mitochondrial cytopathy1259609008
- Chorea due to metabolic disorder1259619002
- Dystonia due to mitochondrial cytopathy1260365000
- Dystonia due to mitochondrial disease1260365000
- Myoclonic disorder due to mitochondrial cytopathy1263505003
- Myoclonic disorder due to mitochondrial disorder1263505003
- Mitochondrial metabolism defect133791000119107
UMLS
Clinical Terms
- Infantile hypertrophic cardiomyopathy due to MRPL44 deficiency
- Hypertrophic mitochondrial cardiomyopathy
- Combined oxidative phosphorylation defect type 16
- Mitochondrial disease
- Myoclonic disorder due to mitochondrial cytopathy
- Non-syndromic mitochondrial sensorineural deafness
- Liver disease co-occurrent and due to mitochondrial disorder
- Chorea due to mitochondrial cytopathy
- Liver disease with mitochondrial disorder
- Mitochondrial metabolism disorders
- Myoclonic disorder due to mitochondrial disorder
- Disorder of glomerulus due to mitochondrial cytopathy
- Chorea due to metabolic disorder
- Demyelination of central nervous system with mitochondrial disorder
- Glomerular disease due to mitochondrial cytopathy
- Mitochondrial metabolism defect
- Infantile hypertrophic cardiomyopathy due to mitochondrial ribosomal protein L44 deficiency
- Demyelination of central nervous system co-occurrent and due to mitochondrial disease
- Mitochondrial cytopathy
- Dystonia due to mitochondrial disease
- Dilated cardiomyopathy due to mitochondrial disease
- Dystonia due to mitochondrial cytopathy
Frequently Asked Questions
What is the ICD-10 code for mitochondrial metabolism disorder, unspecified?
The ICD-10-CM code for mitochondrial metabolism disorder, unspecified is E88.40. The full clinical description is "Mitochondrial metabolism disorder, unspecified". E88.40 is a billable/specific code that can be used on insurance claims and medical billing.
What does ICD-10 code E88.40 mean?
ICD-10-CM code E88.40 represents “Mitochondrial metabolism disorder, unspecified”. 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 E88.40 a billable code?
Yes, E88.40 is a billable/specific ICD-10-CM code and can be used to indicate a diagnosis on a medical claim.
What chapter is E88.40 in?
E88.40 is in Chapter 4: Endocrine, Nutritional and Metabolic Diseases (codes E00-E89).
What codes cannot be used with E88.40?
E88.40 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 E88.40?
Yes, when using E88.40, also report: codes for associated conditions.
What SNOMED CT codes does E88.40 map to?
E88.40 maps to 13 SNOMED CT concepts: 1259619002, 1259609008, 771513008, 724784006, 871639003, and 8 more. SNOMED CT is a clinical terminology used in electronic health records.
What are the UMLS CUIs for E88.40?
E88.40 is linked to 1 UMLS Concept Unique Identifier: C1456275. The UMLS (Unified Medical Language System) integrates multiple biomedical vocabularies maintained by the U.S. National Library of Medicine.
How does E88.40 relate to ICF functioning codes?
ICF (International Classification of Functioning, Disability and Health) codes describe how conditions like mitochondrial metabolism disorder, unspecified 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 E88.40?
There is no direct ICD-11 mapping available for E88.40 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.