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ICD-10-CM Codes
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E00-E89
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E70-E88
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E72-
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2023 ICD-10-CM Diagnosis Code E72.51
2023 ICD-10-CM Diagnosis Code E72.51
Non-ketotic hyperglycinemia
2016 2017 2018 2019 2020 2021 2022 2023 Billable/Specific Code
- E72.51 is a billable/specific ICD-10-CM code that can be used to indicate a diagnosis for reimbursement purposes.
- The 2023 edition of ICD-10-CM E72.51 became effective on October 1, 2022.
- This is the American ICD-10-CM version of E72.51 - other international versions of ICD-10 E72.51 may differ.
The following code(s) above
E72.51 contain annotation back-references
Annotation Back-References
In this context, annotation back-references refer to codes that contain:
- Applicable To annotations, or
- Code Also annotations, or
- Code First annotations, or
- Excludes1 annotations, or
- Excludes2 annotations, or
- Includes annotations, or
- Note annotations, or
- Use Additional annotations
that may be applicable to
E72.51:
- E00-E89
2023 ICD-10-CM Range E00-E89
Endocrine, nutritional and metabolic diseasesNote- All neoplasms, whether functionally active or not, are classified in Chapter 2. Appropriate codes in this chapter (i.e. E05.8, E07.0, E16-E31, E34.-) may be used as additional codes to indicate either functional activity by neoplasms and ectopic endocrine tissue or hyperfunction and hypofunction of endocrine glands associated with neoplasms and other conditions classified elsewhere.
Type 1 Excludes- transitory endocrine and metabolic disorders specific to newborn (P70-P74)
- E70-E88
2023 ICD-10-CM Range E70-E88
Metabolic disordersType 1 Excludes- androgen insensitivity syndrome (E34.5-)
- congenital adrenal hyperplasia (E25.0)
- hemolytic anemias attributable to enzyme disorders (D55.-)
- Marfan's syndrome (Q87.4)
- 5-alpha-reductase deficiency (E29.1)
Type 2 Excludes- Ehlers-Danlos syndromes (Q79.6-)
- E72
ICD-10-CM Diagnosis Code E72
Other disorders of amino-acid metabolism
2016 2017 2018 2019 2020 2021 2022 2023 Non-Billable/Non-Specific Code
Type 1 Excludes- 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.-)
- Hyperglycinemia, non ketotic
Clinical Information
- An autosomal recessive inherited metabolic disorder caused by mutations in the amt and gldc genes. It is characterized by abnormal accumulation of glycine in the brain and other tissues. Signs and symptoms include lethargy, feeding difficulties, hypotonia, intellectual deformities, and seizures.
- An autosomal recessive metabolic disorder caused by deficiencies in the mitochondrial glycine cleavage system.
ICD-10-CM E72.51 is grouped within Diagnostic Related Group(s) (MS-DRG v40.0):
- 642 Inborn and other disorders of metabolism
Convert E72.51 to ICD-9-CM
Code History
- 2016 (effective 10/1/2015): New code (first year of non-draft ICD-10-CM)
- 2017 (effective 10/1/2016): No change
- 2018 (effective 10/1/2017): No change
- 2019 (effective 10/1/2018): No change
- 2020 (effective 10/1/2019): No change
- 2021 (effective 10/1/2020): No change
- 2022 (effective 10/1/2021): No change
- 2023 (effective 10/1/2022): No change
- Disorder (of) - see also Disease
- glycine metabolism E72.50
ICD-10-CM Diagnosis Code E72.50
Disorder of glycine metabolism, unspecified
2016 2017 2018 2019 2020 2021 2022 2023 Billable/Specific Code
- non-ketotic hyperglycinemia E72.51
- metabolism NOS E88.9
ICD-10-CM Diagnosis Code E88.9
Metabolic disorder, unspecified
2016 2017 2018 2019 2020 2021 2022 2023 Billable/Specific Code
- amino-acid E72.9
ICD-10-CM Diagnosis Code E72.9
Disorder of amino-acid metabolism, unspecified
2016 2017 2018 2019 2020 2021 2022 2023 Billable/Specific Code
- glycine E72.50
ICD-10-CM Diagnosis Code E72.50
Disorder of glycine metabolism, unspecified
2016 2017 2018 2019 2020 2021 2022 2023 Billable/Specific Code
- non-ketotic hyperglycinemia E72.51
- Glucoglycinuria E72.51
- Glycinemia E72.51
- Hyperglycinemia E72.51 (non-ketotic)
- Non-ketotic hyperglycinemia E72.51
ICD-10-CM Codes Adjacent To E72.51
E72.2 Disorders of urea cycle metabolism
E72.20 Disorder of urea cycle metabolism, unspecified
E72.22 Arginosuccinic aciduria
E72.29 Other disorders of urea cycle metabolism
E72.3 Disorders of lysine and hydroxylysine metabolism
E72.4 Disorders of ornithine metabolism
E72.5 Disorders of glycine metabolism
E72.50 Disorder of glycine metabolism, unspecified
E72.51
Non-ketotic hyperglycinemia
E72.59 Other disorders of glycine metabolism
E72.8 Other specified disorders of amino-acid metabolism
E72.81 Disorders of gamma aminobutyric acid metabolism
E72.89 Other specified disorders of amino-acid metabolism
E72.9 Disorder of amino-acid metabolism, unspecified
E73.0 Congenital lactase deficiency
E73.1 Secondary lactase deficiency
Reimbursement claims with a date of service on or after October 1, 2015 require the use of ICD-10-CM codes.
