| Dataset | OMIM Gene-Disease Associations |
| Category | disease or phenotype associations |
| Type | phenotype |
| 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://www.omim.org/entry/222700 |
| Similar Terms | |
| Downloads & Tools |
1 genes associated with the lysinuric protein intolerance phenotype from the curated OMIM Gene-Disease Associations dataset.
| Symbol | Name |
|---|---|
| SLC7A7 | solute carrier family 7 (amino acid transporter light chain, y+L system), member 7 |
