Glutaric aciduria, type 2   22886006

SNOMED CT code


SNOMED code22886006
nameGlutaric aciduria, type 2
statusactive
date introduced2002-01-31
fully specified name(s)Glutaric aciduria, type 2 (disorder)
synonyms
  • Glutaric aciduria, type 2
  • Ethylmalonic-adipicaciduria
  • Glutaric acidemia, type 2
  • MADD - multiple acyl-CoA dehydrogenase deficiency
  • Glutaric aciduria type II
  • MAD - Multiple acyl-CoA dehydrogenase deficiency
  • Glutaric acidaemia, type 2
attributes - group1
OccurrenceCongenital   255399007
parents
  • Glutaric aciduria   28987007
  • Disorder of fatty acid metabolism   39929009
  • Autosomal recessive hereditary disorder   85995004
children
  • Alpha chain electron transfer flavoprotein deficiency   1187542000
  • Autosomal recessive glutaric aciduria, type 2   25425008  removed: 2021-09-30
  • Beta chain electron transfer flavoprotein deficiency   1187541007
  • Electron transfer flavoprotein-ubiquinone oxidoreductase deficiency   1187534001
  • X-linked glutaric aciduria, type 2   22062008  removed: 2021-09-30
hierarchies
a selection of possible paths
SNOMED CT Concept   138875005
  Clinical finding   404684003
    Disease   64572001
      Metabolic disease   75934005
        Disorder of organic acid metabolism   116021002
          Non-amino organic acidemia AND/OR aciduria   26513001
            Glutaric aciduria   28987007
              Glutaric aciduria, type 2   22886006

SNOMED CT Concept   138875005
  Clinical finding   404684003
    Disease   64572001
      Metabolic disease   75934005
        Disorder of organic acid metabolism   116021002
          Disorder of fatty acid metabolism   39929009
            Glutaric aciduria, type 2   22886006

SNOMED CT Concept   138875005
  Clinical finding   404684003
    Disease   64572001
      Genetic disease   782964007
        Hereditary disease   32895009
          Autosomal hereditary disorder   1899006
            Autosomal recessive hereditary disorder   85995004
              Glutaric aciduria, type 2   22886006

ancestors
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