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 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
- •cystinosisE72.04
- •cystinuriaE72.01
- •transcobalamin II deficiencyD51.2
Related Codes(3)
Also Known As / Clinical Terms(189)
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
Clinical Terms
- SULFITE OXIDASE DEFICIENCY, ISOLATED
- SULFOCYSTEINURIA
- Deficiency of Cobalamin E
- Hypermethioninaemia due to deficiency of glycine N-methyltransferase
- Inherited disorder of folate metabolism
- Hypermethioninemia due to deficiency of glycine N-methyltransferase
- Hypermethioninemia due to GNMT (glycine N-methyltransferase) deficiency
- Deficiency of Cobalamin G
- Hawkinsinuria
- HPD-gene related hawkinsinuria
- Hypermethioninaemia
- Cystathioninaemia
- Deficiency of methionyl-tRNA synthetase
- Deficiency of methionine-tRNA ligase
- Isolated sulfite oxidase deficiency
- Deficiency of glutamate formiminotransferase
- Smith-Strang disease
- Cystathioninuria (disorder)
- Deficiency of glutathione synthase
- 4-Hydroxyphenylpyruvate dioxygenase deficiency
- Developmental delay, immunodeficiency, leukoencephalopathy, hypohomocysteinemia syndrome
- R-binder deficiency
- MTO (methanethiol oxidase) deficiency
- Hypermethioninemia encephalopathy due to deficiency of adenosine kinase
- Glutamate formiminotransferase deficiency
- Hypermethioninaemia due to GNMT (glycine N-methyltransferase) deficiency
- Transcobalamin I deficiency
- Deficiency of methionine-transfer ribonucleic acid ligase
- Deficiency of homocysteine desulfhydrase
- Sulphite oxidase deficiency syndrome
- hypermethioninemia
- Autosomal recessive extra-oral halitosis
- Cystathionine gamma-lyase deficiency syndrome
- Cystathioninuria
- Deficiency of thetin-homocysteine methyltransferase
- Hypermethioninemia (disorder)
- Inborn error of amino acid metabolism
- Developmental delay, immunodeficiency, leucoencephalopathy, hypohomocysteinemia syndrome
- Oast-house urine disease
- Sulphite oxidase deficiency
- 4-Hydroxyphenylpyruvate hydroxylase deficiency
- Neonatal hypermethioninemia
- Sulphocysteinuria
- Oasthouse disease
- Hypermethioninemia encephalopathy due to ADK (adenosine kinase) deficiency
- CTH - Cystathioninuria
- Deficiency of homocysteine desulphydrase
- Deficiency of glutathione-homocystine transhydrogenase
- Deficiency of cystathionase
- Hypermethioninaemia encephalopathy due to ADK (adenosine kinase) deficiency
- MAT deficiency
- Amino acid below reference range
- THF methyltransferase deficiency
- Deficiency of methionine adenosyltransferase
- Sulfite oxidase deficiency
- Sulfite oxidase deficiency syndrome
- Familial methionine malabsorption
- Oast-house disease
- MET
- Gamma-cystathionase deficiency
- Deficiency of cysteine desulfhydrase
- Hypermethioninaemia encephalopathy due to deficiency of adenosine kinase
- Neonatal hypermethioninaemia
- Deficiency of homoserine deaminase
- Tetrahydrofolate methyltransferase deficiency
- Hepatic methionine adenosyltransferase deficiency
- FIGLUria
- High urine cystathionine levels
- Methioninemia
- Deficiency of glutathione thiolesterase
- ISOD
- Cystathionine gamma-lyase deficiency
- Decreased amino acid
- Hyperaminoaciduria
- Deficiency of cysteine desulphydrase
- Methanethiol oxidase deficiency
- Deficiency of cystine desulphydrase
- Functional defects of methionine synthase
- Cystathioninemia
- Formiminoglutamic aciduria
- Deficiency of cystine desulfhydrase
- Deficiency of glutamate formyltransferase
- Glycine N-methyltransferase deficiency
- Methionine malabsorption syndrome
- Methionine adenosyltransferase deficiency
- Increased methionine in blood
- Sulfite oxidase deficiency (disorder)
- Deficiency of glutathione synthetase
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.
How does E72.19 relate to ICF functioning codes?
ICF (International Classification of Functioning, Disability and Health) codes describe how conditions like other disorders of sulfur-bearing amino-acid 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 E72.19?
There is no direct ICD-11 mapping available for E72.19 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.