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Search all medical codes
E88.40
Mitochondrial metabolism disorder, unspecified
ICD10CM code
Medical Policies and Guidelines for Mitochondrial metabolism disorder, unspecified
Related policies from health plans
OSCAR
Enteral and Oral Liquid Nutritional Supplements (CG011)
CIGNA
Transthoracic Echocardiography in Children - (0523)
SUNFLOWER
Concert Genetic Testing: Metabolic Endocrine Mitochondrial Disorders (PDF)
Similar Codes
ICD10CM codes
E88.40
- Mitochondrial metabolism disorder, unspecified
E88.30
- Mitochondrial metabolism disorder, unspecified
E88.4
- Mitochondrial metabolism disorders
E88.39
- Other mitochondrial metabolism disorders
E88.9
- Metabolic disorder, unspecified
E88.49
- Other mitochondrial metabolism disorders
E88
- Other and unspecified metabolic disorders
E88.89
- Other specified metabolic disorders
E88.8
- Other specified metabolic disorders
E70.20
- Disorder of tyrosine metabolism, unspecified
HCPCS codes
S9435
- Medical foods for inborn errors of metabolism
G9842
- Patient has metastatic disease at diagnosis
G9918
- Functional status not performed, reason not otherwise specified
G8960
- Clinician treating major depressive disorder did not communicate to clinician treating comorbid cond
G8947
- One or more neuropsychiatric symptoms
G6044
- Cocaine or metabolite
G9012
- Other specified case management service not elsewhere classified
G9097
- Oncology; disease status; esophageal cancer, limited to adenocarcinoma or squamous cell carcinoma as
G9322
- Count of previous ct and cardiac nuclear medicine (myocardial perfusion) studies not documented in t
G8959
- Clinician treating major depressive disorder communicates to clinician treating comorbid condition
CPT4 codes
81121
- IDH2 (isocitrate dehydrogenase 2 [NADP+], mitochondrial) (eg, glioma), common variants (eg, R140W, R
81460
- Whole mitochondrial genome (eg, Leigh syndrome, mitochondrial encephalomyopathy, lactic acidosis, an
83570
- Isocitric dehydrogenase (IDH)
81120
- IDH1 (isocitrate dehydrogenase 1 [NADP+], soluble) (eg, glioma), common variants (eg, R132H, R132C)
89240
- Unlisted miscellaneous pathology test
84210
- Pyruvate
81205
- BCKDHB (branched-chain keto acid dehydrogenase E1, beta polypeptide) (eg, maple syrup urine disease)
81425
- Genome (eg, unexplained constitutional or heritable disorder or syndrome); sequence analysis
83874
- Myoglobin
82373
- Carbohydrate deficient transferrin
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