| Dataset | CTD Gene-Disease Associations |
| Category | disease or phenotype associations |
| Type | disease |
| 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) |
| External Link | http://ctdbase.org/detail.go?type=disease&acc=MESH:C562687 |
| Similar Terms | |
| Downloads & Tools |
1 genes/proteins associated with the disease Lysinuric Protein Intolerance from the curated CTD Gene-Disease Associations dataset.
| Symbol | Name | Standardized Value |
|---|---|---|
| SLC7A7 | solute carrier family 7 (amino acid transporter light chain, y+L system), member 7 | 2.88009 |
