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      • 1        Disorders of amino acid metabolism
        • 1.11    Disorders of amino acid transport
          • Iminoglycinuria
          • Hartnup disease
          • Proton-coupled amino acid transporter 2 deficiency
          • Proline imino transporter-asssociated disease
          • Cystinuria
          • Lysinuric protein intolerance
          • Glutamate aspartate transporter deficiency
          • Astroglial glutamate aspartate transporter deficiency
          • Dicarboxylic aminoaciduria
          • Large neutral amino acid transporter deficiency
          • Sodium-coupled neutral amino acid transporter 3 deficiency
          • Neuronal system A amino acid transporter deficiency
          • Vesicular neutral amino acid transporter 3 deficiency
          • Cystinosis
          • Lysosomal cationic amino acid transporter deficiency
          • Cationic amino acid transporter 2 deficiency
          • Cationic amino acid transporter 3 deficiency
          • GABA transporter deficiency
          • Taurine transporter deficiency
          • ASCT1 transporter deficiency
          • Dibasic aminoaciduria type 1
          • Blue diaper syndrome
          • Lysine malabsorption syndrome
          • Histidinuria
          • Methionine malabsorption syndrome
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  • Pathways
  • Multimers
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    • About Online IMD
OnlineIMD
  • Home
  • Diseases
    • INTERMEDIARY METABOLISM: NUTRIENTS
      • 1        Disorders of amino acid metabolism
        • 1.11    Disorders of amino acid transport
          • Iminoglycinuria
          • Hartnup disease
          • Proton-coupled amino acid transporter 2 deficiency
          • Proline imino transporter-asssociated disease
          • Cystinuria
          • Lysinuric protein intolerance
          • Glutamate aspartate transporter deficiency
          • Astroglial glutamate aspartate transporter deficiency
          • Dicarboxylic aminoaciduria
          • Large neutral amino acid transporter deficiency
          • Sodium-coupled neutral amino acid transporter 3 deficiency
          • Neuronal system A amino acid transporter deficiency
          • Vesicular neutral amino acid transporter 3 deficiency
          • Cystinosis
          • Lysosomal cationic amino acid transporter deficiency
          • Cationic amino acid transporter 2 deficiency
          • Cationic amino acid transporter 3 deficiency
          • GABA transporter deficiency
          • Taurine transporter deficiency
          • ASCT1 transporter deficiency
          • Dibasic aminoaciduria type 1
          • Blue diaper syndrome
          • Lysine malabsorption syndrome
          • Histidinuria
          • Methionine malabsorption syndrome
  • Genes
  • Gene products
  • Pathways
  • Multimers
  • More information
    • About Online IMD

Dibasic aminoaciduria type 1

  • Type
    Phenotype
  • External link(s)
    • IEMbase
  • Disease group(s)
    • 1.11    Disorders of amino acid transport