|Dataset||CTD Gene-Disease Associations|
|Category||disease or phenotype associations|
|Description||Lysinuric protein intolerance (LPI) is a very rare inherited multisystem condition caused by distrubance in amino acid metabolism. (Orphanet Rare Disease Ontology, Orphanet_470)|
|Downloads & Tools|
1 genes/proteins associated with the disease Lysinuric Protein Intolerance from the curated CTD Gene-Disease Associations dataset.
|SLC7A7||solute carrier family 7 (amino acid transporter light chain, y+L system), member 7||2.88009|