E72.51
BillableNon-ketotic hyperglycinemia
Non-ketotic hyperglycinemia
Coding Notes
Excludes 1
Codes that cannot be used together with this code (mutual exclusion)
- transitory endocrine and metabolic disorders specific to newborn (P70-P74)
- androgen insensitivity syndrome (E34.5-)
- congenital adrenal hyperplasia (E25.0)
- hemolytic anemias attributable to enzyme disorders (D55.-)
- Marfan syndrome (Q87.4-)
- 5-alpha-reductase deficiency (E29.1)
- disorders of:
- aromatic amino-acid metabolism (E70.-)
- branched-chain amino-acid metabolism (E71.0-E71.2)
- fatty-acid metabolism (E71.3)
- purine and pyrimidine metabolism (E79.-)
- gout (M1A.-, M10.-)
Excludes 2
Conditions not included here, but the patient may have both
- Ehlers-Danlos syndromes (Q79.6-)
Also Known As / Clinical Terms
SNOMED CT
- Glucoglycinuria9111008
- Glucosuria45154002
- Glycosuria45154002
- Transient neonatal hyperglycinaemia51097006
- Transient neonatal hyperglycinemia51097006
- Glycine decarboxylase deficiency63329001
- Glycine dehydrogenase (decarboxylating) deficiency63329001
- Glycine dehydrogenase decarboxylating deficiency63329001
- Non-ketotic hyperglycinaemia P protein deficiency63329001
- Non-ketotic hyperglycinaemia type I63329001
- Non-ketotic hyperglycinemia P protein deficiency63329001
- Non-ketotic hyperglycinemia type I63329001
- Nonketotic hyperglycinaemia, type I63329001
- Nonketotic hyperglycinemia, type I63329001
- P protein deficiency63329001
- P-protein deficiency63329001
- Hyperglycinaemia64654004
- Hyperglycinemia64654004
- Aminomethyltransferase deficiency67845009
- Non-ketotic hyperglycinaemia T protein deficiency67845009
- Non-ketotic hyperglycinaemia type II67845009
- Non-ketotic hyperglycinemia T protein deficiency67845009
- Non-ketotic hyperglycinemia type II67845009
- Nonketotic hyperglycinaemia, type II67845009
- Nonketotic hyperglycinemia, type II67845009
- T protein deficiency67845009
- T-protein deficiency67845009
- Tetrahydrofolate aminomethyltransferase deficiency67845009
- Disorder of glycine cleavage enzyme complex237939006
- NKH - Non-ketotic hyperglycinaemia237939006
- NKH - Non-ketotic hyperglycinemia237939006
- Non ketotic hyperglycinaemia237939006
- Non ketotic hyperglycinemia237939006
- Non-ketotic hyperglycinaemia237939006
- Non-ketotic hyperglycinemia237939006
- Non-ketotic hyperglycinaemia H protein deficiency303092001
- Non-ketotic hyperglycinaemia type III303092001
- Non-ketotic hyperglycinemia H protein deficiency303092001
- Non-ketotic hyperglycinemia type III303092001
- Non-ketotic hyperglycinaemia L protein deficiency303093006
- Non-ketotic hyperglycinaemia type IV303093006
- Non-ketotic hyperglycinemia L protein deficiency303093006
- Non-ketotic hyperglycinemia type IV303093006
- Childhood-onset spasticity with hyperglycinaemia773492007
- Childhood-onset spasticity with hyperglycinemia773492007
- Childhood-onset spasticity with variant non-ketotic hyperglycinaemia773492007
- Childhood-onset spasticity with variant non-ketotic hyperglycinemia773492007
- Spasticity, ataxia, gait anomalies syndrome773492007
- Spastic ataxia1119357005
- Atypical glycine encephalopathy1156791007
- Atypical non-ketotic hyperglycinaemia1156791007
- Atypical non-ketotic hyperglycinemia1156791007
- Neonatal glycine encephalopathy1156803005
- Neonatal non-ketotic hyperglycinaemia1156803005
- Neonatal non-ketotic hyperglycinemia1156803005
- Infantile glycine encephalopathy1156826003
- Infantile non-ketotic hyperglycinaemia1156826003
- Infantile non-ketotic hyperglycinemia1156826003
- Neonatal metabolic acidaemia16068331000119102
- Neonatal metabolic acidemia16068331000119102
UMLS
- Disorder of glycine cleavage enzyme complexC0751748
- Encephalopathies, GlycineC0751748
- Encephalopathy, GlycineC0751748
- GCEC0751748
- GCE1C0751748
- GLYCINE ENCEPHALOPATHY 1C0751748
- Glycine EncephalopathiesC0751748
- Glycine EncephalopathyC0751748
- Glycine encephalopathyC0751748
- HYPERGLYCINEMIA, NONKETOTICC0751748
- Hyperglycinemia, Non-ketoticC0751748
- Hyperglycinemia, NonketoticC0751748
- Hyperglycinemias, Non-ketoticC0751748
- Hyperglycinemias, NonketoticC0751748
- NKHC0751748
- NKH - Non-ketotic hyperglycinaemiaC0751748
- NKH - Non-ketotic hyperglycinemiaC0751748
- Non ketotic HyperglycinemiaC0751748
- Non ketotic hyperglycinaemiaC0751748
- Non ketotic hyperglycinemiaC0751748
- Non-ketotic HyperglycinemiaC0751748
- Non-ketotic HyperglycinemiasC0751748
- Non-ketotic hyperglycinaemiaC0751748
- Non-ketotic hyperglycinemiaC0751748
- Non-ketotic hyperglycinemia (disorder)C0751748
- Nonketotic HyperglycinemiaC0751748
- Nonketotic HyperglycinemiasC0751748
- Nonketotic hyperglycinaemiaC0751748
- Nonketotic hyperglycinemiaC0751748
- non-ketotic hyperglycinaemiaC0751748
- non-ketotic hyperglycinemiaC0751748
- nonketotic hyperglycinemiaC0751748
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.
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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.