Human Phenotype Ontology 
Grandparent Node:
expandAbnormality of the spleen (HP:0001743)help
Parent Node:
expandAbnormal spleen morphology (HP:0025408)help
..Starting node
..expandSplenic abscess (HP:0025059)help
Term ID: 25059
Name: Splenic abscess
Synonym:
Definition: A circumscribed area of pus or necrotic debris in the parenchyma of the spleen.
Comments:
Reference: HP:0025059
Genes and Diseases:
 
       Child Nodes:
........expandMultifocal splenic abscess (HP:0025060) help
........expandUnifocal splenic abscess (HP:0025061) help

 Sister Nodes: 
..expandAplasia/Hypoplasia of the spleen (HP:0010451) help
..expandEctopia of the spleen (HP:0010452) help
..expandHepatosplenomegaly (HP:0001433) help
..expandSplenic cyst (HP:0030423) help
..expandSplenic rupture (HP:0012223) help
..expandSplenogonadal fusion (HP:0025410) help
..expandSplenomegaly (HP:0001744) help
..expandSupernumerary spleens (HP:0009799) 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:0025059HP:0025059Splenic abscess0 CL E G H
HP:0025059HP:0025061Unifocal splenic abscess1 CL E G H
HP:0025059HP:0025060Multifocal splenic abscess1 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.