ICD·index Chapters ENESDE
5C50.B category

Disorders of methionine cycle or sulphur amino acid metabolism

Also indexed as

5-methyltetrahydrofolate-homocysteine s-methyltransferase deficiencyBeery-baby syndromeBrain demyelination due to methionine adenosyltransferase deficiencyCBS - [Cystathionine beta-synthase] deficiencyCTH - [cystathioninuria]Classical homocystinuriaCombined deficiency of sulfite oxidase, xanthine dehydrogenase and aldehyde oxidaseCystathione gamma-lyase deficiencyCystathionine beta-synthase deficiencyCystathioninemiaCystathioninuriaDeficiency of cystathionaseDeficiency of cysteine desulfhydraseDeficiency of homoserine deaminaseDeficiency of methionine adenosyltransferaseDisorders of methionine cycle or sulphur amino acid metabolismDisorders of sulphur-bearing amino-acid metabolismEncephalopathy due to sulfite oxidase deficiencyFamilial methionine malabsorptionGNMT - [Glycine N-methyltransferase] deficiencyGamma-cystathionase deficiencyGlycine N-methyltransferase deficiencyHepatic methionine adenosyltransferase deficiencyHomocystinaemiaHomocystinuria - megaloblastic anaemia due to defect in cobalamin metabolism, cbI E complementation typeHomocystinuria - megaloblastic anaemia due to defect in cobalamin metabolism, cbI G complementation typeHomocystinuria due to cystathionine beta-synthase deficiencyHomocystinuria due to defect in methylation type cbl EHomocystinuria due to methionine synthase deficiency type Cbl GHomocystinuria without methylmalonic aciduriaHypermethioninaemiaHypermethioninaemia due to S-adenosylhomocysteine hydrolase deficiencyHypermethioninaemia due to adenosine kinase deficiencyISOD - [Isolated sulfite oxidase deficiency]Isolated persistent hypermethioninaemiaIsolated sulfite oxidase deficiencyMAT I/III - [Methionine adenosyltransferase I/III] deficiencyMethionine adenosyltransferase I/III deficiencyMethionine malabsorption syndromeMethionine synthase deficiencyMethylcobalamin deficiencyMethylcobalamin deficiency type cbl Dv1Methylcobalamin deficiency type cbl EMethylcobalamin deficiency type cbl GMolybdenum cofactor deficiency due to defects in MOCS1 geneMolybdenum cofactor deficiency due to defects in MOCS2 geneMolybdenum cofactor deficiency, complementation group AMolybdenum cofactor deficiency, complementation group BMolybdenum cofactor deficiency, complementation group CN5-methylhomocysteine transferase deficiencyOther genetic defects of methionine cycle or sulfur amino acid metabolismPsychomotor retardation and myopathy due to S-adenosylhomocysteine hydrolase deficiencySecondary non-genetic disorders of methionine cycle or sulfur amino acid metabolismSmith-Strang diseaseSulfite oxidase deficiencySulfite oxidase deficiency due to molybdenum cofactor deficiencycystathionine metabolic disordercystathionine synthase deficiencydeficiency of cysteine desulphydrasedeficiency of cystine desulfhydrasedeficiency of cystine desulphydrasedisorder of sulphur-bearing amino acid including those due to folate and b12 disturbancedisorder of sulphur-bearing amino acid metabolismdisorder of transsulfurationdisorder of transsulphurationdisturbances of sulphur-bearing amino-acid metabolismhomocystine metabolic disordermethionine metabolic disorderoast-house diseaseoast-house urine diseaseoasthouse diseaseoasthouse urine diseasesulfite oxidase deficiency syndromesulfocysteinuriasulphite oxidase deficiencysulphocysteinuriasulphuraminoacidaemia

Nearby in Inborn errors of amino acid or other organic acid metabolism