AutoICD API

E72.51

Billable

Non-ketotic hyperglycinemia

Non-ketotic hyperglycinemia

Status

Billable / Specific

Block

E70-E88

Parent Code

E72.5

Coding Notes

Excludes 1

Codes that cannot be used together with this code (mutual exclusion)

Excludes 2

Conditions not included here, but the patient may have both

Related Codes(4)
E72.50

Disorder of glycine metabolism, unspecified

BillableE72.52

Trimethylaminuria

BillableE72.53

Primary hyperoxaluria

BillableE72.59

Other disorders of glycine metabolism

Billable
Also Known As / Clinical Terms(168)

SNOMED CT

UMLS

Clinical Terms

  • Non-ketotic hyperglycinaemia type I
  • Childhood-onset spasticity with variant non-ketotic hyperglycinaemia
  • Infantile non-ketotic hyperglycinaemia
  • Spastic ataxia
  • Glycine dehydrogenase (decarboxylating) deficiency
  • Hyperglycinemia
  • Non-ketotic hyperglycinaemia type II
  • Nonketotic Hyperglycinemia
  • Transient neonatal hyperglycinemia
  • Glycine encephalopathy
  • Non-ketotic hyperglycinemia T protein deficiency
  • Non-ketotic hyperglycinaemia
  • Non-ketotic hyperglycinaemia type III
  • Hyperglycinemia, Nonketotic
  • Atypical non-ketotic hyperglycinaemia
  • Non-ketotic hyperglycinemia H protein deficiency
  • Non ketotic hyperglycinaemia
  • T protein deficiency
  • Non-ketotic hyperglycinaemia type IV
  • NKH - Non-ketotic hyperglycinemia
  • Glycine dehydrogenase decarboxylating deficiency
  • Neonatal metabolic acidemia
  • Non-ketotic hyperglycinemia type II
  • Hyperglycinemia, Non-ketotic
  • Glycosuria
  • Non-ketotic hyperglycinaemia P protein deficiency
  • Transient neonatal hyperglycinaemia
  • Non-ketotic hyperglycinemia type I
  • Neonatal non-ketotic hyperglycinaemia
  • Infantile non-ketotic hyperglycinemia
  • GCE
  • Non-ketotic hyperglycinemia type III
  • Childhood-onset spasticity with hyperglycinemia
  • Non-ketotic hyperglycinemia type IV
  • Infantile glycine encephalopathy
  • Non ketotic hyperglycinemia
  • Aminomethyltransferase deficiency
  • Nonketotic hyperglycinemia, type II
  • NKH
  • Nonketotic hyperglycinaemia
  • Spasticity, ataxia, gait anomalies syndrome
  • Neonatal metabolic acidaemia
  • Disorder of glycine cleavage enzyme complex
  • NKH - Non-ketotic hyperglycinaemia
  • Neonatal non-ketotic hyperglycinemia
  • Non-ketotic hyperglycinaemia H protein deficiency
  • Encephalopathies, Glycine
  • Non-ketotic hyperglycinemia P protein deficiency
  • Non-ketotic hyperglycinaemia T protein deficiency
  • Non-ketotic Hyperglycinemias
  • Glucosuria
  • Childhood-onset spasticity with variant non-ketotic hyperglycinemia
  • Glucoglycinuria
  • GCE1
  • Atypical non-ketotic hyperglycinemia
  • Hyperglycinemias, Non-ketotic
  • Nonketotic Hyperglycinemias
  • Glycine Encephalopathies
  • Glycine decarboxylase deficiency
  • Hyperglycinaemia
  • Tetrahydrofolate aminomethyltransferase deficiency
  • T-protein deficiency
  • Childhood-onset spasticity with hyperglycinaemia
  • P-protein deficiency
  • Non-ketotic hyperglycinemia (disorder)
  • GLYCINE ENCEPHALOPATHY 1
  • Nonketotic hyperglycinemia, type I
  • P protein deficiency
  • Nonketotic hyperglycinaemia, type I
  • Encephalopathy, Glycine
  • Neonatal glycine encephalopathy
  • Hyperglycinemias, Nonketotic
  • Nonketotic hyperglycinaemia, type II
  • Non-ketotic hyperglycinaemia L protein deficiency
  • Non-ketotic hyperglycinemia L protein deficiency
  • Atypical glycine encephalopathy
Frequently Asked Questions
What is the ICD-10 code for non-ketotic hyperglycinemia?

The ICD-10-CM code for non-ketotic hyperglycinemia is E72.51. The full clinical description is "Non-ketotic hyperglycinemia". E72.51 is a billable/specific code that can be used on insurance claims and medical billing.

What does ICD-10 code E72.51 mean?

ICD-10-CM code E72.51 represents “Non-ketotic hyperglycinemia”. It is classified under Chapter 4: Endocrine, Nutritional and Metabolic Diseases and is a billable/specific code that can be used on a claim.

Is E72.51 a billable code?

Yes, E72.51 is a billable/specific ICD-10-CM code and can be used to indicate a diagnosis on a medical claim.

What chapter is E72.51 in?

E72.51 is in Chapter 4: Endocrine, Nutritional and Metabolic Diseases (codes E00-E89).

What codes cannot be used with E72.51?

E72.51 has Excludes1 notes indicating codes that cannot be used together with it, including: transitory endocrine and metabolic disorders specific to newborn (P70-P74); androgen insensitivity syndrome (E34.5-); congenital adrenal hyperplasia (E25.0); and 9 more.

What SNOMED CT codes does E72.51 map to?

E72.51 maps to 15 SNOMED CT concepts: 67845009, 1156791007, 773492007, 237939006, 9111008, and 10 more. SNOMED CT is a clinical terminology used in electronic health records.

What are the UMLS CUIs for E72.51?

E72.51 is linked to 1 UMLS Concept Unique Identifier: C0751748. The UMLS (Unified Medical Language System) integrates multiple biomedical vocabularies maintained by the U.S. National Library of Medicine.

How does E72.51 relate to ICF functioning codes?

ICF (International Classification of Functioning, Disability and Health) codes describe how conditions like non-ketotic hyperglycinemia affect a person's functioning — body functions, activities, participation, and environmental factors. AutoICD provides ICF Core Sets for 12+ conditions and can map clinical text to ICF categories automatically. Browse the ICF directory to explore functioning codes.

What is the ICD-11 equivalent of E72.51?

There is no direct ICD-11 mapping available for E72.51 in the WHO crosswalk tables. This may mean the concept is classified differently in ICD-11. Use the ICD-10 to ICD-11 converter to search for related codes.

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Includes SNOMED Clinical Terms® (SNOMED CT®) used by permission of SNOMED International. Includes content from the UMLS Metathesaurus, courtesy of the U.S. National Library of Medicine.