Amino acid transport disorder   16784003

SNOMED CT code


SNOMED code16784003
nameAmino acid transport disorder
statusactive
date introduced2002-01-31
fully specified name(s)Amino acid transport disorder (disorder)
synonyms
  • Amino acid transport disorder
  • Disorder of amino acid transport
parents
  • Metabolic disorder of transport   111394006
  • Disorder of amino acid and organic acid metabolism   237911005
children
  • Amino acid transport disorder NOS   190686008  removed: 2010-01-31
  • Autosomal recessive cerebellar ataxia, pyramidal signs, nystagmus, oculomotor apraxia syndrome   763312008
  • Cystinemia   190682005
  • Cystinosis   190681003
  • Cystinuria   85020001
  • Dicarboxylic aminoaciduria syndrome   716747007
  • Fanconi syndrome   40488004
  • Glucoaminophosphaturia syndrome   44673006  removed: 2021-07-31
  • Histidine transport defect   78311009
  • Iminoglycinuria   84121007
  • Lowe syndrome   79385002
  • Lysinuric protein intolerance   303852004
  • Neonatal cystine-lysinuria   30101004
  • Neutral 1 amino acid transport defect   80902009
  • Other specified amino acid transport disorder   267416002  removed: 2010-01-31
hierarchies
a selection of possible paths
SNOMED CT Concept   138875005
  Clinical finding   404684003
    Disease   64572001
      Metabolic disease   75934005
        Metabolic disorder of transport   111394006
          Amino acid transport disorder   16784003

SNOMED CT Concept   138875005
  Clinical finding   404684003
    Disease   64572001
      Metabolic disease   75934005
        Disorder of organic acid metabolism   116021002
          Disorder of amino acid metabolism   44779003
            Disorder of amino acid and organic acid metabolism   237911005
              Amino acid transport disorder   16784003

ancestors
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