Human Phenotype Ontology 
Grandparent Node:
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Morphological abnormality of the gastrointestinal tract (HP:0012718)help
Parent Node:
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Abnormal esophagus morphology (HP:0002031)help
..Starting node
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Esophageal leukoplakia (HP:0012859)help
Term ID: 12859
Name: Esophageal leukoplakia
Synonym: Esophageal epidermoid metaplasia
Definition: A white patch or plaque occurring on the surface of the esophageal mucous membranes that cannot be rubbed off and cannot be characterized clinically as any other disease.
Comments:
Reference: HP:0012859
Genes and Diseases:
 
       Child Nodes:

 Sister Nodes: 
..expandAcute esophageal necrosis (HP:0011128) help
..expandEsophageal atresia (HP:0002032) help
..expandEsophageal diverticulum (HP:0100628) help
..expandEsophageal duplication (HP:0100681) help
..expandEsophageal furrows (HP:0031858) 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:0012859HP:0012859Esophageal leukoplakia0 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.