Human Phenotype Ontology 
Grandparent Node:
expandAbnormal esophagus morphology (HP:0002031)help
Grandparent Node:
expandGastrointestinal inflammation (HP:0004386)help
Parent Node:
expandEsophagitis (HP:0100633)help
..Starting node
..expandEosinophilic microabscess formation in the esophagus (HP:0410152)help
Term ID: 410152
Name: Eosinophilic microabscess formation in the esophagus
Synonym: Eosinophilic micro-abscess formation in the esophagus; Eosinophilic micro-abscess formation in the oesophagus; Eosinophilic microabscess formation in the oesophagus
Definition: The formation of small localized collection of eosinophiles (an eosinophilic microabscess) in the esophagus. Usually clusters of greater than or equal to 4 eosinophils are seen, that appear as exudates or white spots or white plaques.
Comments:
Reference: HP:0410152
Genes and Diseases:
 
       Child Nodes:

 Sister Nodes: 
..expandEosinophilic infiltration of the esophagus (HP:0410151) 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:0410152HP:0410152Eosinophilic microabscess formation in the esophagus0 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.