Neutral 1 Amino Acid Transport Defect
| Disease Aliases (16) | Amino acid transport disorder, neutral Aminoaciduria Aminoaciduria, hartnup type Deficiency of tryptophan 2,3-dioxygenase Deficiency of tryptophan pyrrolase Hartnup disease Hnd Hartnup disorder Hartnup disorder; hnd Hartnup type Neutral 1 amino acid transport defect Neutral amino acid transport defect Neutral amino acid transport disorder Transport disorder, neutral amino acid Transport disorder, neutral amino acids Deficiency of tryptophan oxygenase |
Associated Genes (2) NCBI-RefSeq: CLTRN (Collectrin, amino acid transport regulator) External Links: gnomAD browser Ensembl GeneCards
NCBI-RefSeq: SLC6A19 (Solute carrier family 6 member 19) External Links: gnomAD browser Ensembl GeneCards
| |||||||
| Cross-references of Neutral 1 amino acid transport defect | OMIM | GARD | Orphanet | NCBI-GTR | NCBI-MedGen | MalaCards | MeSH | Annotations | |