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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
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