E72.19
BillableOther disorders of sulfur-bearing amino-acid metabolism
Other disorders of sulfur-bearing amino-acid metabolism
Coding Notes
Inclusion Terms
Alternative clinical terms for this condition
- Cystathioninuria
- Methioninemia
- Sulfite oxidase deficiency
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.-)
- cystinosis (E72.04)
- cystinuria (E72.01)
- transcobalamin II deficiency (D51.2)
Excludes 2
Conditions not included here, but the patient may have both
- Ehlers-Danlos syndromes (Q79.6-)
Also Known As / Clinical Terms
SNOMED CT
- Inherited disorder of folate metabolism4702003
- Cystathioninaemia6669004
- Cystathioninemia6669004
- Cystathionine gamma-lyase deficiency6885006
- Deficiency of cystathionase6885006
- Deficiency of cysteine desulfhydrase6885006
- Deficiency of cysteine desulphydrase6885006
- Deficiency of cystine desulfhydrase6885006
- Deficiency of cystine desulphydrase6885006
- Deficiency of homoserine deaminase6885006
- Gamma-cystathionase deficiency6885006
- CTH - Cystathioninuria13003007
- Cystathionine gamma-lyase deficiency syndrome13003007
- Cystathioninuria13003007
- Neonatal hypermethioninaemia37695001
- Neonatal hypermethioninemia37695001
- Sulfite oxidase deficiency syndrome40873003
- Sulfocysteinuria40873003
- Sulphite oxidase deficiency syndrome40873003
- Sulphocysteinuria40873003
- Hyperaminoaciduria42930003
- Inborn error of amino acid metabolism42930003
- Hypermethioninaemia43123004
- Hypermethioninemia43123004
- Familial methionine malabsorption45812003
- Methionine malabsorption syndrome45812003
- Oast-house disease45812003
- Oast-house urine disease45812003
- Oasthouse disease45812003
- Smith-Strang disease45812003
- Hepatic methionine adenosyltransferase deficiency57835009
- MAT deficiency57835009
- Methionine adenosyltransferase deficiency57835009
- Deficiency of glutamate formiminotransferase59761008
- Deficiency of glutamate formyltransferase59761008
- FIGLUria59761008
- Formiminoglutamic aciduria59761008
- Glutamate formiminotransferase deficiency59761008
- THF methyltransferase deficiency89579000
- Tetrahydrofolate methyltransferase deficiency89579000
- Amino acid below reference range124057005
- Decreased amino acid124057005
- Deficiency of glutathione-homocystine transhydrogenase124197006
- Deficiency of thetin-homocysteine methyltransferase124240001
- Deficiency of methionine adenosyltransferase124283007
- Deficiency of glutathione thiolesterase124430002
- Deficiency of homocysteine desulfhydrase124633009
- Deficiency of homocysteine desulphydrase124633009
- Deficiency of methionine-tRNA ligase124696003
- Deficiency of methionine-transfer ribonucleic acid ligase124696003
- Deficiency of methionyl-tRNA synthetase124696003
- Deficiency of glutathione synthase124706000
- Deficiency of glutathione synthetase124706000
- R-binder deficiency237933007
- Transcobalamin I deficiency237933007
- Deficiency of Cobalamin E237937008
- Deficiency of Cobalamin G237938003
- Functional defects of methionine synthase360376008
- Sulfite oxidase deficiency367368009
- Sulphite oxidase deficiency367368009
- 4-Hydroxyphenylpyruvate dioxygenase deficiency413356003
- 4-Hydroxyphenylpyruvate hydroxylase deficiency413356003
- HPD-gene related hawkinsinuria414380008
- Hawkinsinuria414380008
- Glycine N-methyltransferase deficiency763720007
- Hypermethioninaemia due to GNMT (glycine N-methyltransferase) deficiency763720007
- Hypermethioninaemia due to deficiency of glycine N-methyltransferase763720007
- Hypermethioninemia due to GNMT (glycine N-methyltransferase) deficiency763720007
- Hypermethioninemia due to deficiency of glycine N-methyltransferase763720007
- Hypermethioninaemia encephalopathy due to ADK (adenosine kinase) deficiency763721006
- Hypermethioninaemia encephalopathy due to deficiency of adenosine kinase763721006
- Hypermethioninemia encephalopathy due to ADK (adenosine kinase) deficiency763721006
- Hypermethioninemia encephalopathy due to deficiency of adenosine kinase763721006
- Autosomal recessive extra-oral halitosis1269235004
- MTO (methanethiol oxidase) deficiency1269235004
- Methanethiol oxidase deficiency1269235004
- Developmental delay, immunodeficiency, leucoencephalopathy, hypohomocysteinemia syndrome1340174002
- Developmental delay, immunodeficiency, leukoencephalopathy, hypohomocysteinemia syndrome1340174002
UMLS
- CTH - CystathioninuriaC0220993
- CYSTATHIONINURIAC0220993
- Cystathionine gamma-lyase deficiency syndromeC0220993
- CystathioninuriaC0220993
- Cystathioninuria (disorder)C0220993
- High urine cystathionine levelsC0220993
- cystathioninuriaC0220993
- HypermethioninaemiaC4048705
- HypermethioninemiaC4048705
- Hypermethioninemia (disorder)C4048705
- Increased methionine in bloodC4048705
- METC4048705
- MethioninemiaC4048705
- hypermethioninaemiaC4048705
- hypermethioninemiaC4048705
- ISODC0268624
- Isolated sulfite oxidase deficiencyC0268624
- SULFITE OXIDASE DEFICIENCY, ISOLATEDC0268624
- SULFOCYSTEINURIAC0268624
- Sulfite oxidase deficiencyC0268624
- Sulfite oxidase deficiency (disorder)C0268624
- Sulphite oxidase deficiencyC0268624
- Other disorders of sulfur-bearing amino-acid metabolismC2874260
Frequently Asked Questions
What is the ICD-10 code for other disorders of sulfur-bearing amino-acid metabolism?
The ICD-10-CM code for other disorders of sulfur-bearing amino-acid metabolism is E72.19. The full clinical description is "Other disorders of sulfur-bearing amino-acid metabolism". E72.19 is a billable/specific code that can be used on insurance claims and medical billing.
What does ICD-10 code E72.19 mean?
ICD-10-CM code E72.19 represents "Other disorders of sulfur-bearing amino-acid 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 E72.19 a billable code?
Yes, E72.19 is a billable/specific ICD-10-CM code and can be used to indicate a diagnosis on a medical claim.
What chapter is E72.19 in?
E72.19 is in Chapter 4: Endocrine, Nutritional and Metabolic Diseases (codes E00-E89).
What codes cannot be used with E72.19?
E72.19 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 12 more.
What SNOMED CT codes does E72.19 map to?
E72.19 maps to 31 SNOMED CT concepts: 413356003, 124057005, 1269235004, 13003007, 6669004, and 26 more. SNOMED CT is a clinical terminology used in electronic health records.
What are the UMLS CUIs for E72.19?
E72.19 is linked to 4 UMLS Concept Unique Identifiers: C0220993, C4048705, C0268624, C2874260. 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.