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Search all medical codes
E88.4
Mitochondrial metabolism disorders
ICD10CM code
Similar Codes
ICD10CM codes
E88.4
- Mitochondrial metabolism disorders
E88.39
- Other mitochondrial metabolism disorders
E88.40
- Mitochondrial metabolism disorder, unspecified
E88.49
- Other mitochondrial metabolism disorders
E88.30
- Mitochondrial metabolism disorder, unspecified
E88.8
- Other specified metabolic disorders
E88.9
- Metabolic disorder, unspecified
E88.89
- Other specified metabolic disorders
E88
- Other and unspecified metabolic disorders
E88.81
- Metabolic syndrome
HCPCS codes
S9435
- Medical foods for inborn errors of metabolism
G9842
- Patient has metastatic disease at diagnosis
G6044
- Cocaine or metabolite
G8947
- One or more neuropsychiatric symptoms
G8959
- Clinician treating major depressive disorder communicates to clinician treating comorbid condition
S3620
- Newborn metabolic screening panel, includes test kit, postage and the laboratory tests specified by
G8980
- Mobility: walking & moving around functional limitation, discharge status, at discharge from therapy
G8485
- I intend to report the diabetes mellitus (dm) measures group
G6042
- Amphetamine or methamphetamine
G8960
- Clinician treating major depressive disorder did not communicate to clinician treating comorbid cond
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)
83874
- Myoglobin
84210
- Pyruvate
81440
- Nuclear encoded mitochondrial genes (eg, neurologic or myopathic phenotypes), genomic sequence panel
81205
- BCKDHB (branched-chain keto acid dehydrogenase E1, beta polypeptide) (eg, maple syrup urine disease)
82373
- Carbohydrate deficient transferrin
83090
- Homocysteine
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