Other disorders of amino-acid metabolism
In Metabolic disorders (E70-E88), chapter 4: Endocrine, Nutritional and Metabolic Diseases
31 billable codes under E72: 27 are a CC; 3 map to HCC 50 (Amyloidosis, Porphyria, and Other Specified Metabolic Disorders).A CC or MCC (major CC) is a secondary diagnosis that raises the MS-DRG payment. An HCC counts toward a Medicare Advantage patient's risk score.
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Instructional notes
Also applies, from Metabolic disorders (E70-E88)
These notes sit on E70-E88 and apply to every code under it, including E72.
Excludes1: not coded here, use a different code
Excludes2: not included here, code separately if applicable
- Ehlers-Danlos syndromes (Q79.6-)
Official coding guidelines
From the ICD-10-CM Official Guidelines for Coding and Reporting, FY 2027 (CMS and NCHS). Links open the PDF at the right page.
Covers diabetes mellitus coding, including type, insulin and drug use, pump malfunction and secondary diabetes, plus obesity and obesity class codes.
- Diabetes mellitus (page 39)
- Obesity (page 42)
All codes under E72
E72 can't be used on a claim. Pick a billable code below; grey headings group them.
- E72.0Disorders of amino-acid transport
- E72.00Disorders of amino-acid transport, unspecified
- E72.01Cystinuria
- E72.02Hartnup's disease
- E72.03Lowe's syndrome
- E72.04Cystinosis
- E72.09Other disorders of amino-acid transport
- E72.1Disorders of sulfur-bearing amino-acid metabolism
- E72.10Disorders of sulfur-bearing amino-acid metabolism, unspecified
- E72.11Homocystinuria
- E72.12Methylenetetrahydrofolate reductase deficiency
- E72.19Other disorders of sulfur-bearing amino-acid metabolism
- E72.2Disorders of urea cycle metabolism
- E72.20Disorder of urea cycle metabolism, unspecified
- E72.21Argininemia
- E72.22Arginosuccinic aciduria
- E72.23Citrullinemia
- E72.29Other disorders of urea cycle metabolism
- E72.3Disorders of lysine and hydroxylysine metabolism
- E72.4Disorders of ornithine metabolism
- E72.5Disorders of glycine metabolism
- E72.50Disorder of glycine metabolism, unspecified
- E72.51Non-ketotic hyperglycinemia
- E72.52Trimethylaminuria
- E72.53Primary hyperoxaluria
- E72.530Primary hyperoxaluria, type 1
- E72.538Other specified primary hyperoxaluria
- E72.539Primary hyperoxaluria, unspecified
- E72.54Secondary hyperoxaluria
- E72.540Dietary hyperoxaluria
- E72.541Enteric hyperoxaluria
- E72.548Other secondary hyperoxaluria
- E72.549Secondary hyperoxaluria, unspecified
- E72.59Other disorders of glycine metabolism
- E72.8Other specified disorders of amino-acid metabolism
- E72.81Disorders of gamma aminobutyric acid metabolism
- E72.89Other specified disorders of amino-acid metabolism
- E72.9Disorder of amino-acid metabolism, unspecified
E72 MS-DRGs
As the principal diagnosis, the billable codes under E72 group to MS-DRG 642, 695, or 696 (v44.0). Which one applies depends on procedures performed, secondary diagnoses (CC/MCC), and the patient's age and discharge status.
- DRG 642 Inborn and Other Disorders of Metabolism (27 of 31 codes)
- DRG 695 Kidney and Urinary Tract Signs and Symptoms with MCC (4 of 31 codes)
- DRG 696 Kidney and Urinary Tract Signs and Symptoms without MCC (4 of 31 codes)
Other codes that refer to E72
Notes on these codes point to E72.
About the condition
Plain-language background from MedlinePlus (National Library of Medicine), not coding guidance.
Amino Acid Metabolism Disorders
Metabolism is the process your body uses to make energy from the food you eat. Food is made up of proteins, carbohydrates, and fats. Your digestive system breaks the food parts down into sugars and acids, your body's fuel. Your body can use this fuel right away, or it can store the energy in your body. If you have a metabolic disorder, something goes wrong with this process.
Read more about amino acid metabolism disorders on MedlinePlusCode history
Valid since FY2016, when ICD-10-CM took effect on October 1, 2015. No changes since.
