lysinuric protein intolerance

Summary
Synonym
  • LPI
  • dibasic amino aciduria II
  • hyperdibasic aminoaciduria
Definition
An amino acid metabolic disorder characterized by the body's inability to effectively break down lysine, arginine and ornithine and by renal hyperdiaminoaciduria, especially lysinuria, and by impaired formation of urea with hyperammonemia after protein ingestion. It has_material_basis_in homozygous or compound heterozygous mutation in the amino acid transporter gene SLC7A7 on chromosome 14q11.
Super Class
amino acid metabolic disorder
External Links
Disease Ontology
DOID:0060439
Mondo Disease Ontology
MeSH
UMLS
NCI Thesaurus
ORDO
OMIM
GARD
MGI genotype (from TogoID)
WikiPathways (from TogoID)
Related Genes
Displaying 1 entry
Gene ID Gene Symbol Description Source
9056 SLC7A7 solute carrier family 7 member 7
Displaying 1 entry
Gene ID Gene Symbol Description Source
20540 Slc7a7 solute carrier family 7 (cationic amino acid transporter, y+ system), member 7
Displaying 1 entry
Gene ID Gene Symbol Description Source
83509 Slc7a7 solute carrier family 7 member 7

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Acknowledgements

Supported by JST NBDC Grant Number JPMJND2204

Partly supported by NIH Common Fund Grant #1U01GM125267-01


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Last updated: August 19, 2024