Human Phenotype Ontology 
Grandparent Node:
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Abnormal esophagus morphology (HP:0002031)help
Grandparent Node:
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Neoplasm of head and neck (HP:0012288)help
Grandparent Node:
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Neoplasm of the gastrointestinal tract (HP:0007378)help
Parent Node:
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Esophageal neoplasm (HP:0100751)help
..Starting node
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Esophageal carcinoma (HP:0011459)help
Term ID: 11459
Name: Esophageal carcinoma
Synonym:
Definition: The presence of a carcinoma of the esophagus.
Comments:
Reference: HP:0011459
Genes and Diseases:
 
       Child Nodes:

 Sister Nodes: 
..expandBarrett esophagus (HP:0100580) help
..expandEsophageal squamous papilloma (HP:0031463) help
InputHPO IDHPO termDistanceGeneGene id entrezDiseaseIdDiseaseNameDiseaseMIMConceptIDSourceTypical associationHGMD variantsClinVar variantsHGNC IDGeneMIM
 
HPO disease - gene - phenotype typical associations:
HP:0011459HP:0011459Esophageal carcinoma0ASCC1 CL E G H51008614266Barrett esophagus614266C0004763OMIM18224268614215
HP:0011459HP:0011459Esophageal carcinoma0ASCC1 CL E G H51008614266Barrett esophagus614266C0004763OMIM16324268614215
HP:0011459HP:0011459Esophageal carcinoma0CTHRC1 CL E G H115908614266Barrett esophagus614266C0004763OMIM13918831610635
HP:0011459HP:0011459Esophageal carcinoma0CTHRC1 CL E G H115908614266Barrett esophagus614266C0004763OMIM13718831610635
HP:0011459HP:0011459Esophageal carcinoma0DLEC1 CL E G H994099977ORPHA1412899604050
HP:0011459HP:0011459Esophageal carcinoma0DLEC1 CL E G H994099977ORPHA1392899604050
HP:0011459HP:0011459Esophageal carcinoma0MSR1 CL E G H4481614266Barrett esophagus614266C0004763OMIM11067376153622
HP:0011459HP:0011459Esophageal carcinoma0RHBDF2 CL E G H79651148500Howel-Evans syndrome148500C1835664OMIM117020788614404
HP:0011459HP:0011459Esophageal carcinoma0RHBDF2 CL E G H79651148500Howel-Evans syndrome148500C1835664OMIM116720788614404
HP:0011459HP:0011459Esophageal carcinoma0RNF6 CL E G H604999977ORPHA13910069604242
HP:0011459HP:0011459Esophageal carcinoma0RNF6 CL E G H604999977ORPHA14110069604242
HP:0011459HP:0011459Esophageal carcinoma0TGFBR2 CL E G H704899977ORPHA175011773190182
HP:0011459HP:0011459Esophageal carcinoma0TGFBR2 CL E G H704899977ORPHA169411773190182
HP:0011459HP:0011459Esophageal carcinoma0WWOX CL E G H5174199977ORPHA176712799605131
HP:0011459HP:0011459Esophageal carcinoma0WWOX CL E G H5174199977ORPHA187912799605131
 
HPO disease - gene - phenotype less frequent non-typical associations:
HP:0011459HP:0011459Esophageal carcinoma0APC CL E G H32479665ORPHA09051583611731
HP:0011459HP:0011459Esophageal carcinoma0APC CL E G H324247806ORPHA09963583611731
HP:0011459HP:0011459Esophageal carcinoma0APC CL E G H324247806ORPHA09051583611731
HP:0011459HP:0011459Esophageal carcinoma0APC CL E G H32479665ORPHA09963583611731
HP:0011459HP:0011459Esophageal carcinoma0STAT1 CL E G H6772391487ORPHA031411362600555
HP:0011459HP:0011459Esophageal carcinoma0STAT1 CL E G H6772391487ORPHA036811362600555


Genes (10) :APC ASCC1 CTHRC1 DLEC1 MSR1 RHBDF2 RNF6 STAT1 TGFBR2 WWOX

Diseases (6) :247806 79665 614266 99977 148500 391487
 

Human Phenotype Ontology(HPO) is developed by the Human Phenotype Ontology Consortium. The version used here is August 2021 release.