Human Phenotype Ontology 
Grandparent Node:
expandNephrolithiasis (HP:0000787)help
Parent Node:
expandCalcium nephrolithiasis (HP:0004724)help
..Starting node
..expandCalcium oxalate nephrolithiasis (HP:0008672)help
Term ID: 8672
Name: Calcium oxalate nephrolithiasis
Synonym: Ca oxalate kidney stone; Ca oxalate nephrolithiasis; Ca oxalate urolithiasis; Ca2+ oxalate kidney stone; Ca2+ oxalate nephrolithiasis; Ca2+ oxalate urolithiasis; Calcium oxalate kidney stones; Calcium oxalate urolithiasis; Oxalate nephrolithiasis
Definition: The presence of calcium- and oxalate-containing calculi (stones) in the kidneys.
Comments:
Reference: HP:0008672
Genes and Diseases:
 
       Child Nodes:

 Sister Nodes: 
..expandCalcium phosphate nephrolithiasis (HP:0012580) 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:0008672HP:0008672Calcium oxalate nephrolithiasis0ADCY10 CL E G H5581121285OMIM:143870Hypercalciuria, absorptive, susceptibility to.5
HP:0008672HP:0008672Calcium oxalate nephrolithiasis0ADCY10 CL E G H5581121285ORPHA:2197Idiopathic hypercalciuriaHP:0040282 - Frequent5
HP:0008672HP:0008672Calcium oxalate nephrolithiasis0AGXT CL E G H189341OMIM:259900Hyperoxaluria, primary, type I.260
HP:0008672HP:0008672Calcium oxalate nephrolithiasis0GRHPR CL E G H93804570OMIM:260000Hyperoxaluria, primary, type II.70
HP:0008672HP:0008672Calcium oxalate nephrolithiasis0HOGA1 CL E G H11281725155OMIM:613616HYPEROXALURIA, PRIMARY, TYPE III; HP383
HP:0008672HP:0008672Calcium oxalate nephrolithiasis0HOGA1 CL E G H11281725155ORPHA:93600Primary hyperoxaluria type 3HP:0040281 - Very frequent83
HP:0008672HP:0008672Calcium oxalate nephrolithiasis0OPLAH CL E G H268738149OMIM:2600055-@oxoprolinase deficiency.5
HP:0008672HP:0008672Calcium oxalate nephrolithiasis0SLC26A1 CL E G H1086110993OMIM:167030Nephrolithiasis, calcium oxalate.24
HP:0008672HP:0008672Calcium oxalate nephrolithiasis0SLC36A2 CL E G H15320118762OMIM:138500Glycinuria with or without oxalate urolithiasis.2
HP:0008672HP:0008672Calcium oxalate nephrolithiasis0SLC6A19 CL E G H34002427960OMIM:138500Glycinuria with or without oxalate urolithiasis.12
HP:0008672HP:0008672Calcium oxalate nephrolithiasis0SLC6A20 CL E G H5471630927OMIM:138500Glycinuria with or without oxalate urolithiasis.96


Genes (9) :ADCY10 AGXT GRHPR HOGA1 OPLAH SLC26A1 SLC36A2 SLC6A19 SLC6A20

Diseases (9) :OMIM:143870 ORPHA:2197 OMIM:259900 OMIM:260000 OMIM:613616 ORPHA:93600 OMIM:260005 OMIM:167030 OMIM:138500
 

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