Human Phenotype Ontology 
Grandparent Node:
expandAbnormality of amino acid metabolism (HP:0004337)help
Grandparent Node:
expandAciduria (HP:0012072)help
Parent Node:
expandAbnormal circulating lysine concentration (HP:0010908)help
Parent Node:
expandAminoaciduria (HP:0003355)help
..Starting node
..expandHyperlysinuria (HP:0003297)help
Term ID: 3297
Name: Hyperlysinuria
Synonym: High urine lysine levels; Lysinuria
Definition: An increased concentration of lysine in the urine.
Comments:
Reference: HP:0003297
Genes and Diseases:
 
       Child Nodes:

 Sister Nodes: 
..expand3-Methylglutaconic aciduria (HP:0003535) help
..expandArgininuria (HP:0003268) help
..expandCarnosinuria (HP:0003167) help
..expandComplex organic aciduria (HP:0008336) help
..expandCystathioninuria (HP:0003153) help
..expandCystinuria (HP:0003131) help
..expandDiaminoaciduria (HP:0008339) help
..expandDibasicaminoaciduria (HP:0003168) help
..expandElevated urinary aminoisobutyric acid (HP:0045034) help
..expandGeneralized aminoaciduria (HP:0002909) help
..expandHistidinuria (HP:0002927) help
..expandHomocystinuria (HP:0002156) help
..expandHydroxyprolinuria (HP:0003080) help
..expandHyperglutaminuria (HP:0025376) help
..expandHyperglycinuria (HP:0003108) help
..expandHyperthreoninuria (HP:0003296) help
..expandIncreased urinary taurine (HP:0003166) help
..expandLacticaciduria (HP:0003648) help
..expandNeutral hyperaminoaciduria (HP:0008353) help
..expandobsolete Renal aminoaciduria (HP:0008335) help
..expandOrnithinuria (HP:0003532) help
..expandPhosphohydroxylysinuria (HP:0031870) help
..expandProlinuria (HP:0003137) help
..expandTransient aminoaciduria (HP:0008273) help
..expandTryptophanuria (HP:0003361) help
InputHPO IDHPO termDistanceGeneGene id entrezHGNC IDDiseaseIdDiseaseNameFrequencyOnsetHGMD variantsClinVar variants
 
HPO disease - gene - phenotype typical associations:
 
HPO disease - gene - phenotype less frequent non-typical associations:
HP:0003297HP:0003297Hyperlysinuria0AASS CL E G H1015717366ORPHA:2203HyperlysinemiaHP:0040282 - Frequent15
HP:0003297HP:0003297Hyperlysinuria0AASS CL E G H1015717366ORPHA:3124SaccharopinuriaHP:0040282 - Frequent15
HP:0003297HP:0003297Hyperlysinuria0SLC3A1 CL E G H651911025OMIM:220100CYSTINURIA.55
HP:0003297HP:0003297Hyperlysinuria0SLC7A7 CL E G H905611065ORPHA:470Lysinuric protein intoleranceHP:0040282 - Frequent104
HP:0003297HP:0003297Hyperlysinuria0SLC7A9 CL E G H1113611067OMIM:220100CYSTINURIA.58


Genes (4) :AASS SLC3A1 SLC7A7 SLC7A9

Diseases (4) :ORPHA:2203 ORPHA:3124 OMIM:220100 ORPHA:470
 

Human Phenotype Ontology(HPO) is developed by the Human Phenotype Ontology Consortium. The version used here is December 15 2022 release.