Lysinuric Protein Intolerance Gene Set

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
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Genes

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