E72.59
BillableOther disorders of glycine metabolism
Other disorders of glycine metabolism
Coding Notes
Inclusion Terms
Alternative clinical terms for this condition
- D-glycericacidemia
- Hyperhydroxyprolinemia
- Hyperprolinemia (types I, II)
- Sarcosinemia
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
- Hyperprolinaemia59655002
- Hyperprolinemia59655002
- Hyperprolinaemia type I61071003
- Hyperprolinaemia, type I61071003
- Hyperprolinemia type I61071003
- Hyperprolinemia, type I61071003
- Proline dehydrogenase deficiency61071003
- Proline oxidase deficiency61071003
- Deficiency of the sarcosine dehydrogenase complex64852002
- Demethylation defect of N-methylglycine64852002
- Hypersarcosinaemia64852002
- Hypersarcosinemia64852002
- Sarcosinaemia64852002
- Sarcosine dehydrogenase deficiency64852002
- Sarcosinemia64852002
- Sarcosinuria64852002
- Deficiency of sarcosine oxidase124181001
- Deficiency of glycine acyltransferase124262001
- Hyperprolinaemia type 2717181004
- Hyperprolinaemia type II717181004
- Hyperprolinemia type 2717181004
- Hyperprolinemia type II717181004
- Deficiency of dimethylglycine dehydrogenase719449007
- Dimethylglycine dehydrogenase deficiency719449007
UMLS
- 4-HYDROXY-L-PROLINE OXIDASE DEFICIENCYC0268531
- 4-Hydroxy-L-Proline Oxidase DeficiencyC0268531
- HYDROXYPROLINEMIAC0268531
- High blood hydroxyproline levelsC0268531
- HydroxyprolinaemiaC0268531
- HydroxyprolinemiaC0268531
- HyperhydroxyprolinaemiaC0268531
- HyperhydroxyprolinemiaC0268531
- Hyperhydroxyprolinemia (disorder)C0268531
- hydroxyprolinaemiaC0268531
- hydroxyprolinemiaC0268531
- D-GLYCERIC ACIDEMIAC1291386
- D-Glycerate kinase deficiencyC1291386
- D-Glyceric AcidemiaC1291386
- D-glycericacidemiaC1291386
- Glycerate Kinase DeficiencyC1291386
- Deficiency of the sarcosine dehydrogenase complexC0268563
- Demethylation defect of N-methylglycineC0268563
- HYPERSARCOSINEMIAC0268563
- High plasma sarcosine levelsC0268563
- HypersarcosinaemiaC0268563
- HypersarcosinemiaC0268563
- SARCOSC0268563
- SARCOSINE DEHYDROGENASE COMPLEX DEFICIENCYC0268563
- SARCOSINEMIAC0268563
- SARD DEFICIENCYC0268563
- SARD DeficiencyC0268563
- SARDH DEFICIENCYC0268563
- SARDH DeficiencyC0268563
- SARDHDC0268563
- Sarcosin dehydrogenase complex, deficiency ofC0268563
- SarcosinaemiaC0268563
- Sarcosine Dehydrogenase Complex, Deficiency OfC0268563
- Sarcosine dehydrogenase deficiencyC0268563
- Sarcosine dehydrogenase deficiency (disorder)C0268563
- SarcosinemiaC0268563
- SarcosinuriaC0268563
- Hyperprolinemia (types I, II)C2874263
- Other disorders of glycine metabolismC2874264
Frequently Asked Questions
What is the ICD-10 code for other disorders of glycine metabolism?
The ICD-10-CM code for other disorders of glycine metabolism is E72.59. The full clinical description is "Other disorders of glycine metabolism". E72.59 is a billable/specific code that can be used on insurance claims and medical billing.
What does ICD-10 code E72.59 mean?
ICD-10-CM code E72.59 represents "Other disorders of glycine metabolism". 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 E72.59 a billable code?
Yes, E72.59 is a billable/specific ICD-10-CM code and can be used to indicate a diagnosis on a medical claim.
What chapter is E72.59 in?
E72.59 is in Chapter 4: Endocrine, Nutritional and Metabolic Diseases (codes E00-E89).
What codes cannot be used with E72.59?
E72.59 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 E72.59 map to?
E72.59 maps to 7 SNOMED CT concepts: 719449007, 124262001, 124181001, 64852002, 59655002, and 2 more. SNOMED CT is a clinical terminology used in electronic health records.
What are the UMLS CUIs for E72.59?
E72.59 is linked to 5 UMLS Concept Unique Identifiers: C0268531, C1291386, C0268563, C2874263, C2874264. 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.