Human Phenotype Ontology 
Grandparent Node:
expandAbnormal nephron morphology (HP:0012575)help
Grandparent Node:
expandAbnormal renal corpuscle morphology (HP:0031263)help
Parent Node:
expandAbnormal renal glomerulus morphology (HP:0000095)help
..Starting node
..expandLobular glomerulopathy (HP:0008636)help
Term ID: 8636
Name: Lobular glomerulopathy
Synonym:
Definition:
Comments:
Reference: HP:0008636
Genes and Diseases:
 
       Child Nodes:

 Sister Nodes: 
..expandAbnormal glomerular capillary morphology (HP:0025006) help
..expandAbnormal glomerular mesangium morphology (HP:0001966) help
..expandGlomerular basement membrane lamellation (HP:0030034) help
..expandGlomerular deposits (HP:0030949) help
..expandGlomerular endocapillary hypercellularity (HP:0025363) help
..expandGlomerular extracapillary hypercellularity (HP:0025364) help
..expandGlomerular sclerosis (HP:0000096) help
..expandGlomerulomegaly (HP:0030162) help
..expandGlomerulonephritis (HP:0000099) help
..expandGlomerulopathy (HP:0100820) help
..expandMultiple glomerular cysts (HP:0100611) help
..expandRenal juxtaglomerular cell hypertrophy/hyperplasia (HP:0000111) help
..expandThickened glomerular basement membrane (HP:0004722) help
..expandThin glomerular basement membrane (HP:0012577) 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:0008636HP:0008636Lobular glomerulopathy0 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.