2026 ICD-10-CM Diagnosis Code E72.51Non-ketotic hyperglycinemia
ICD-10-CM Codes›E00–E89›E70-E88›E72
- Billable — Valid for Submission
- Chronic Condition
E72.51 is a billable ICD-10-CM diagnosis code for non-ketotic hyperglycinemia. It is valid on HIPAA claims for fiscal year 2026 (October 1, 2025 through September 30, 2026). In AHRQ's Clinical Classifications Software (CCSR), this diagnosis falls under Other specified and unspecified nutritional and metabolic disorders.
Code Identity
Code Classification
Approximate SynonymsGuidance
Alternate terms and clinical phrases that map to this code.
- Aminomethyltransferase deficiency
- Atypical glycine encephalopathy
- Childhood-onset spasticity with hyperglycinemia
- Glucoglycinuria
- Glycine dehydrogenase deficiency
- Glycosuria
- Hyperglycinemia
- Infantile glycine encephalopathy
- Neonatal glycine encephalopathy
- Neonatal metabolic acidemia
- Non-ketotic hyperglycinemia
- Non-ketotic hyperglycinemia H protein deficiency
- Non-ketotic hyperglycinemia L protein deficiency
- Spastic ataxia
- Transient neonatal hyperglycinemia
Index to Diseases and InjuriesGuidance
Alphabetical index entries that point to this code.
- Disorder (of) - See Also: Disease;
- non-ketotic hyperglycinemia - E72.51
- metabolism NOS - E88.9
- amino-acid - E72.9
- non-ketotic hyperglycinemia - E72.51
- Glucoglycinuria - E72.51
- Glycinemia - E72.51
- Hyperglycinemia (non-ketotic) - E72.51
- Non-ketotic hyperglycinemia - E72.51
External Cause of Injuries IndexGuidance
References for this code in the External Cause of Injuries Index.
- Disorder(of)
- glycine metabolism
- non-ketotic hyperglycinemia
- Disorder(of)
- metabolism NOS
- amino-acid
- glycine
- non-ketotic hyperglycinemia
- Glucoglycinuria
- Glycinemia
- Hyperglycinemia(non-ketotic)
- Non-ketotic hyperglycinemia
Clinical ClassificationClinical
AHRQ’s CCSR groups this code into broader clinical categories.
Clinical InformationClinical
Glycosuria
the appearance of an abnormally large amount of glucose in the urine, such as more than 500 mg/day in adults. it can be due to hyperglycemia or genetic defects in renal reabsorption (renal glycosuria).Glycosuria, Renal
an autosomal inherited disorder due to defective reabsorption of glucose by the proximal renal tubules. the urinary loss of glucose can reach beyond 50 g/day. it is attributed to the mutations in the sodium-glucose transporter 2 encoded by the slc5a2 gene.
Patient EducationClinical
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.
Read the full article at MedlinePlus
Courtesy of MedlinePlus, a service of the U.S. National Library of Medicine.
Convert E72.51 to ICD-9-CMHistory
The closest ICD-9-CM equivalents under the General Equivalence Mappings.
Code HistoryHistory
Questions About E72.51Overview
Is E72.51 (Disorders of glycine metabolism) a billable code?
Yes. This is a billable ICD-10-CM code, specific enough to report non-ketotic hyperglycinemia on HIPAA-covered claims from October 1, 2025 through September 30, 2026.
What is the ICD-9 equivalent of E72.51?
Under the General Equivalence Mappings, non-ketotic hyperglycinemia converts to ICD-9-CM 270.7 (straig amin-acid met NEC). The mapping is approximate, so confirm the match fits the documentation.
Footnotes
[1] Chronic - a chronic condition code indicates a condition lasting 12 months or longer and its effect on the patient based on one or both of the following criteria:
- The condition results in the need for ongoing intervention with medical products,treatment, services, and special equipment
- The condition places limitations on self-care, independent living, and social interactions.
