- TypeGroup
- Disease group(s)
- Child entries
- Iminoglycinuria
- Glycine transporter 1 deficiency
- Glycine transporter 2 deficiency
- Hartnup disease
- Proton-coupled amino acid transporter 2 deficiency
- Proline imino transporter-asssociated disease
- Cystinuria
- Lysinuric protein intolerance
- Glutamate aspartate transporter deficiency
- Mitochondrial ornithine transporter deficiency
- Astroglial glutamate aspartate transporter deficiency
- Dicarboxylic aminoaciduria
- Aralar deficiency
- Mitochondrial glutamate transporter deficiency
- Citrin deficiency
- Large neutral amino acid transporter deficiency
- S-adenosylmethionine carrier deficiency
- Sodium-coupled neutral amino acid transporter 3 deficiency
- Neuronal system A amino acid transporter deficiency
- Mitochondrial glycine 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