Human Phenotype Ontology 
Grandparent Node:
expandAbnormality of the kidney (HP:0000077)help
Parent Node:
expandAbnormal renal morphology (HP:0012210)help
..Starting node
..expandDecreased renal parenchymal thickness (HP:0025327)help
Term ID: 25327
Name: Decreased renal parenchymal thickness
Synonym:
Definition: Reduced dimension of the solid part of the kidney (parenchyma, the renal cortex and medulla) as measured from the collecting system (renal calyces and pelvis) to the border of the kidney. This measurement can be performed by measuring the thickness of the parenchyma in computed tomography scans.
Comments:
Reference: HP:0025327
Genes and Diseases:
 
       Child Nodes:

 Sister Nodes: 
..expandAbnormal localization of kidney (HP:0100542) help
..expandAbnormal nephron morphology (HP:0012575) help
..expandAbnormal renal artery morphology (HP:0008776) help
..expandAbnormal renal calyx morphology (HP:0011130) help
..expandAbnormal renal collecting system morphology (HP:0004742) help
..expandAbnormal renal cortex morphology (HP:0011035) help
..expandAbnormal renal medulla morphology (HP:0100957) help
..expandAbnormal renal pelvis morphology (HP:0010944) help
..expandEnlarged kidney (HP:0000105) help
..expandHyperechogenic kidneys (HP:0004719) help
..expandNephrocalcinosis (HP:0000121) help
..expandNephrogenic rest (HP:0100880) help
..expandNephrolithiasis (HP:0000787) help
..expandNephrosclerosis (HP:0009741) help
..expandPerinephric fluid collection (HP:0031226) help
..expandPerirenal hematoma (HP:0030171) help
..expandRenal amyloidosis (HP:0001917) help
..expandRenal atrophy (HP:0012585) help
..expandRenal cyst (HP:0000107) help
..expandRenal duplication (HP:0000075) help
..expandRenal dysplasia (HP:0000110) help
..expandRenal fibrosis (HP:0030760) help
..expandRenal hypoplasia/aplasia (HP:0008678) help
..expandRenal malrotation (HP:0004712) help
..expandRenal steatosis (HP:0000799) 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:0025327HP:0025327Decreased renal parenchymal thickness0 CL E G H


Genes (0) :

Diseases (0) :
 

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