lysinuric protein intolerance Gene Set

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

Genes

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