Human Phenotype Ontology 
Grandparent Node:
expandMorphological abnormality of the gastrointestinal tract (HP:0012718)help
Parent Node:
expandAbnormal esophagus morphology (HP:0002031)help
..Starting node
..expandAcute esophageal necrosis (HP:0011128)help
Term ID: 11128
Name: Acute esophageal necrosis
Synonym:
Definition: A condition characterized by necrosis of the mucosal and submucosal layers of the esophagus not related to ingestion of caustic or other injurious agents. Endoscopically, there is a dark lesion ('black esophagus') distributed in a circumferential manner in the distal one-third of the esophagus with or without exudates. There is involvement of the distal esophagus ending sharply at the gastroesophageal junction.
Comments:
Reference: HP:0011128
Genes and Diseases:
 
       Child Nodes:

 Sister Nodes: 
..expandEsophageal atresia (HP:0002032) help
..expandEsophageal diverticulum (HP:0100628) help
..expandEsophageal duplication (HP:0100681) help
..expandEsophageal furrows (HP:0031858) help
..expandEsophageal leukoplakia (HP:0012859) help
..expandEsophageal neoplasm (HP:0100751) help
..expandEsophageal obstruction (HP:0005240) help
..expandEsophageal stenosis (HP:0010450) help
..expandEsophageal ulceration (HP:0004791) help
..expandEsophageal varix (HP:0002040) help
..expandEsophageal web (HP:0100594) help
..expandEsophagitis (HP:0100633) help
..expandSpontaneous esophageal perforation (HP:0005203) help
..expandTracheoesophageal fistula (HP:0002575) 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:0011128HP:0011128Acute esophageal necrosis0 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.