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Disease Ontology Browser
lysinuric protein intolerance (DOID:0060439)
Alliance: disease page
Synonyms: dibasic amino aciduria II; hyperdibasic aminoaciduria; LPI
Alt IDs: OMIM:222700, MESH:C562687, NCI:C121563, ORDO:470, UMLS_CUI:C0268647
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.

Disease References using Mouse Models (1)
Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO)
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11/12/2024
MGI 6.24 		The Jackson Laboratory