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 newbornP70-P74
- •androgen insensitivity syndromeE34.5
- •congenital adrenal hyperplasiaE25.0
- •hemolytic anemias attributable to enzyme disordersD55
- •Marfan syndromeQ87.4
- •5-alpha-reductase deficiencyE29.1
- disorders of:
- •aromatic amino-acid metabolismE70
- •branched-chain amino-acid metabolismE71.0-E71.2
- •fatty-acid metabolismE71.3
- •purine and pyrimidine metabolismE79
- •gout (M1A.-,M10
Related Codes(4)
Also Known As / Clinical Terms(108)
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
Clinical Terms
- Hypersarcosinemia
- Proline oxidase deficiency
- Sarcosinemia
- 4-HYDROXY-L-PROLINE OXIDASE DEFICIENCY
- Sarcosine dehydrogenase deficiency (disorder)
- Sarcosinuria
- Hyperprolinemia
- Hyperprolinaemia type 2
- Hyperprolinemia, type I
- Sarcosine dehydrogenase deficiency
- Proline dehydrogenase deficiency
- SARCOS
- SARD DEFICIENCY
- Sarcosin dehydrogenase complex, deficiency of
- HYDROXYPROLINEMIA
- D-Glycerate kinase deficiency
- Hyperhydroxyprolinemia (disorder)
- Deficiency of dimethylglycine dehydrogenase
- High plasma sarcosine levels
- D-glycericacidemia
- High blood hydroxyproline levels
- hydroxyprolinaemia
- Sarcosinaemia
- Hyperprolinaemia type II
- Hyperprolinemia type I
- Hyperprolinemia type 2
- Hyperprolinaemia
- Deficiency of glycine acyltransferase
- Hyperprolinemia (types I, II)
- Deficiency of sarcosine oxidase
- SARCOSINE DEHYDROGENASE COMPLEX DEFICIENCY
- SARDH Deficiency
- D-Glyceric Acidemia
- SARDHD
- Glycerate Kinase Deficiency
- Hyperprolinaemia, type I
- Hypersarcosinaemia
- Hyperhydroxyprolinemia
- Dimethylglycine dehydrogenase deficiency
- Sarcosine Dehydrogenase Complex, Deficiency Of
- Hyperhydroxyprolinaemia
- Hyperprolinaemia type I
- Hyperprolinemia type II
- Demethylation defect of N-methylglycine
- Deficiency of the sarcosine dehydrogenase complex
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.
How does E72.59 relate to ICF functioning codes?
ICF (International Classification of Functioning, Disability and Health) codes describe how conditions like other disorders of glycine metabolism 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 E72.59?
There is no direct ICD-11 mapping available for E72.59 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.
Automate ICD-10 Coding With AI
Send clinical text to the AutoICD API and get back structured ICD-10 codes with confidence scores. Integrates into any EHR or billing system in minutes.
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.