277.87 - Disorders Of Mitochondrial Metabolism
The ICD 9 Code for Disorders of mitochondrial metabolism is listed as 277.87.
Additional information concerning this code and description can be found below including ICD 10 crosswalks / GEMS, and chapter information where available.
ICD 9 CM Field | Value |
---|---|
Diagnosis Code: | 277.87 |
Long Description: | Disorders of mitochondrial metabolism |
Short Description: | Dis mitochondrial metab |
Chapter: | Endocrine, Nutritional And Metabolic Diseases, And Immunity Disorders |
Block: | Other Metabolic Disorders And Immunity Disorders (270-279) |
Related Descriptions: |
Juvenile myopathy, encephalopathy, lactic acidosis AND stroke
Kearns-Sayre syndrome Mitochondrial encephalomyopathy Myoclonus epilepsy AND ragged red fibers Neurogenic muscle weakness, ataxia and retinitis pigmentosa Pearson's syndrome |
ICD-10-CM Diagnosis Codes General Equivalence Mappings (GEMS): | |
ICD-10-CM Code: | E88.40 - Mitochondrial metabolism disorder, unspecified (approximate) |
ICD-10-CM Code: | E88.41 - MELAS syndrome (approximate) |
ICD-10-CM Code: | E88.42 - MERRF syndrome (approximate) |
ICD-10-CM Code: | E88.49 - Other mitochondrial metabolism disorders (approximate) |
ICD-10-CM Code: | H49.819 - Kearns-Sayre syndrome, unspecified eye (approximate) |
ICD-9-CM Siblings (same level / similar specificity) of 277.87: | |
277.81 - Primary carnitine deficiency | |
277.82 - Carnitine deficiency due to inborn errors of metabolism | |
277.83 - Iatrogenic carnitine deficiency | |
277.84 - Other secondary carnitine deficiency | |
277.85 - Disorders of fatty acid oxidation | |
277.86 - Peroxisomal disorders | |
277.88 - Tumor lysis syndrome | |
277.89 - Other specified disorders of metabolism |