E88.43
BillableDisorders of mitochondrial tRNA synthetases
Disorders of mitochondrial tRNA synthetases
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(55)
UMLS
- ARS2-related mitochondrial disordersC6007061
- COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 12C4706421
- COXPD12C4706421
- COXPD12 - combined oxidative phosphorylation defect type 12C4706421
- Combined oxidative phosphorylation defect type 12C4706421
- Combined oxidative phosphorylation deficiency 12C4706421
- LEUKOENCEPHALOPATHY WITH THALAMUS AND BRAINSTEM INVOLVEMENT AND HIGH LACTATEC4706421
- LTBLC4706421
- Leukoencephalopathy with thalamus - brainstem involvement - high lactateC4706421
- Leukoencephalopathy with thalamus and brainstem involvement and high lactateC4706421
- Leukoencephalopathy, thalamus and brainstem anomalies, high lactate syndromeC4706421
- Leukoencephalopathy, thalamus and brainstem anomalies, high lactate syndrome (disorder)C4706421
- Disorders of mitochondrial tRNA synthetasesC5819112
- Mitochondrial aminoacyl-tRNA synthetase disordersC5819112
- LBSLC1970180
- LBSL - Leucoencephalopathy with brainstem and spinal cord involvement with lactate elevationC1970180
- LBSL - Leukoencephalopathy with brainstem and spinal cord involvement with lactate elevationC1970180
- LEUKOENCEPHALOPATHY WITH BRAINSTEM AND SPINAL CORD INVOLVEMENT AND LACTATE ELEVATIONC1970180
- Leucoencephalopathy with brain stem and spinal cord involvement and high lactate syndromeC1970180
- Leucoencephalopathy with brain stem and spinal cord involvement and lactate elevation syndromeC1970180
- Leucoencephalopathy with brainstem and spinal cord involvement and lactate elevationC1970180
- Leukoencephalopathy with Brainstem and Spinal Cord Involvement and Lactate ElevationC1970180
- Leukoencephalopathy with brain stem and spinal cord involvement and high lactate syndromeC1970180
- Leukoencephalopathy with brain stem and spinal cord involvement and high lactate syndrome (disorder)C1970180
- Leukoencephalopathy with brain stem and spinal cord involvement and lactate elevation syndromeC1970180
- Leukoencephalopathy with brainstem - spinal cord involvement - lactate elevationC1970180
- Leukoencephalopathy with brainstem and spinal cord involvement and lactate elevationC1970180
- Leukoencephalopathy with brainstem and spinal cord involvement and lactate elevation (disorder)C1970180
- MITOCHONDRIAL ASPARTYL-tRNA SYNTHETASE DEFICIENCYC1970180
- Mitochondrial Aspartyl-tRNA Synthetase DeficiencyC1970180
- Mitochondrial aspartyl-tRNA synthetase deficiencyC1970180
Clinical Terms
- Leukoencephalopathy with thalamus and brainstem involvement and high lactate
- Leukoencephalopathy, thalamus and brainstem anomalies, high lactate syndrome
- Mitochondrial aminoacyl-tRNA synthetase disorders
- Leucoencephalopathy with brain stem and spinal cord involvement and high lactate syndrome
- COXPD12
- Leukoencephalopathy with brain stem and spinal cord involvement and high lactate syndrome (disorder)
- Leukoencephalopathy with brainstem and spinal cord involvement and lactate elevation (disorder)
- Leukoencephalopathy with Brainstem and Spinal Cord Involvement and Lactate Elevation
- Leukoencephalopathy with brain stem and spinal cord involvement and high lactate syndrome
- COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 12
- COXPD12 - combined oxidative phosphorylation defect type 12
- Leukoencephalopathy, thalamus and brainstem anomalies, high lactate syndrome (disorder)
- Leukoencephalopathy with brainstem - spinal cord involvement - lactate elevation
- LBSL - Leucoencephalopathy with brainstem and spinal cord involvement with lactate elevation
- Combined oxidative phosphorylation defect type 12
- MITOCHONDRIAL ASPARTYL-tRNA SYNTHETASE DEFICIENCY
- LBSL
- Leukoencephalopathy with brain stem and spinal cord involvement and lactate elevation syndrome
- LTBL
- ARS2-related mitochondrial disorders
- LBSL - Leukoencephalopathy with brainstem and spinal cord involvement with lactate elevation
- Leucoencephalopathy with brain stem and spinal cord involvement and lactate elevation syndrome
- Leukoencephalopathy with thalamus - brainstem involvement - high lactate
- Leucoencephalopathy with brainstem and spinal cord involvement and lactate elevation
Frequently Asked Questions
What is the ICD-10 code for disorders of mitochondrial trna synthetases?
The ICD-10-CM code for disorders of mitochondrial trna synthetases is E88.43. The full clinical description is "Disorders of mitochondrial tRNA synthetases". E88.43 is a billable/specific code that can be used on insurance claims and medical billing.
What does ICD-10 code E88.43 mean?
ICD-10-CM code E88.43 represents “Disorders of mitochondrial tRNA synthetases”. 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 E88.43 a billable code?
Yes, E88.43 is a billable/specific ICD-10-CM code and can be used to indicate a diagnosis on a medical claim.
What chapter is E88.43 in?
E88.43 is in Chapter 4: Endocrine, Nutritional and Metabolic Diseases (codes E00-E89).
What codes cannot be used with E88.43?
E88.43 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 E88.43?
Yes, when using E88.43, also report: codes for associated conditions.
What are the UMLS CUIs for E88.43?
E88.43 is linked to 4 UMLS Concept Unique Identifiers: C6007061, C4706421, C5819112, C1970180. The UMLS (Unified Medical Language System) integrates multiple biomedical vocabularies maintained by the U.S. National Library of Medicine.
How does E88.43 relate to ICF functioning codes?
ICF (International Classification of Functioning, Disability and Health) codes describe how conditions like disorders of mitochondrial trna synthetases 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 E88.43?
There is no direct ICD-11 mapping available for E88.43 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.