5C50.B Disorders of methionine cycle or sulphur amino acid metabolism
International Classification of Diseases for Mortality and Morbidity Statistics, 11th Revision, v2024-01
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synonyms
- Disorders of methionine cycle or sulphur amino acid metabolism
- disorder of sulphur-bearing amino acid including those due to folate and b12 disturbance
- disorder of sulphur-bearing amino acid metabolism
- disorder of transsulfuration
- disorder of transsulphuration
- disturbances of sulphur-bearing amino-acid metabolism
- sulphuraminoacidaemia
- Disorders of sulphur-bearing amino-acid metabolism
- Brain demyelination due to methionine adenosyltransferase deficiency
- Methionine adenosyltransferase I/III deficiency
- Isolated persistent hypermethioninaemia
- MAT I/III - [Methionine adenosyltransferase I/III] deficiency
- Glycine N-methyltransferase deficiency
- GNMT - [Glycine N-methyltransferase] deficiency
- Psychomotor retardation and myopathy due to S-adenosylhomocysteine hydrolase deficiency
- Hypermethioninaemia due to S-adenosylhomocysteine hydrolase deficiency
- Cystathioninuria
- Gamma-cystathionase deficiency
- Cystathione gamma-lyase deficiency
- CTH - [cystathioninuria]
- cystathionine metabolic disorder
- Classical homocystinuria
- Homocystinuria due to cystathionine beta-synthase deficiency
- Cystathionine beta-synthase deficiency
- CBS - [Cystathionine beta-synthase] deficiency
- cystathionine synthase deficiency
- homocystine metabolic disorder
- Homocystinuria without methylmalonic aciduria
- 5-methyltetrahydrofolate-homocysteine s-methyltransferase deficiency
- Methionine synthase deficiency
- Methylcobalamin deficiency
- N5-methylhomocysteine transferase deficiency
- Methylcobalamin deficiency type cbl E
- Homocystinuria due to defect in methylation type cbl E
- Homocystinuria - megaloblastic anaemia due to defect in cobalamin metabolism, cbI E complementation type
- Methylcobalamin deficiency type cbl G
- Homocystinuria due to methionine synthase deficiency type Cbl G
- Homocystinuria - megaloblastic anaemia due to defect in cobalamin metabolism, cbI G complementation type
- Methylcobalamin deficiency type cbl Dv1
- Encephalopathy due to sulfite oxidase deficiency
- Isolated sulfite oxidase deficiency
- ISOD - [Isolated sulfite oxidase deficiency]
- Sulfite oxidase deficiency due to molybdenum cofactor deficiency
- Combined deficiency of sulfite oxidase, xanthine dehydrogenase and aldehyde oxidase
- Molybdenum cofactor deficiency, complementation group A
- Molybdenum cofactor deficiency due to defects in MOCS1 gene
- Molybdenum cofactor deficiency, complementation group B
- Molybdenum cofactor deficiency due to defects in MOCS2 gene
- Molybdenum cofactor deficiency, complementation group C
- Hypermethioninaemia due to adenosine kinase deficiency
- Other genetic defects of methionine cycle or sulfur amino acid metabolism
- Secondary non-genetic disorders of methionine cycle or sulfur amino acid metabolism
- Beery-baby syndrome
- Cystathioninemia
- Deficiency of cystathionase
- Deficiency of cysteine desulfhydrase
- deficiency of cysteine desulphydrase
- deficiency of cystine desulfhydrase
- deficiency of cystine desulphydrase
- Deficiency of homoserine deaminase
- Deficiency of methionine adenosyltransferase
- Familial methionine malabsorption
- Hepatic methionine adenosyltransferase deficiency
- Homocystinaemia
- Hypermethioninaemia
- methionine metabolic disorder
- Methionine malabsorption syndrome
- oast-house disease
- oast-house urine disease
- oasthouse disease
- oasthouse urine disease
- Smith-Strang disease
- Sulfite oxidase deficiency
- sulfite oxidase deficiency syndrome
- sulphite oxidase deficiency
- sulfocysteinuria
- sulphocysteinuria
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