Human Phenotype Ontology 
Grandparent Node:
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Abnormal ear morphology (HP:0031703)help
Grandparent Node:
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Neoplasm by anatomical site (HP:0011793)help
Parent Node:
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Abnormality of the middle ear (HP:0000370)help
Parent Node:
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Neoplasm of the ear (HP:0012780)help
..Starting node
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Neoplasm of the middle ear (HP:0100799)help
Term ID: 100799
Name: Neoplasm of the middle ear
Synonym: Middle ear tumor; Middle ear tumour; Neoplasia of the middle ear
Definition: A tumor (abnormal growth of tissue) of the middle ear.
Comments:
Reference: HP:0100799
Genes and Diseases:
 
       Child Nodes:
........expandCholesteatoma (HP:0009797) help

 Sister Nodes: 
..expandNeoplasm of the inner ear (HP:0040096) help
..expandNeoplasm of the outer ear (HP:0040095) help
InputHPO IDHPO termDistanceGeneGene id entrezDiseaseIdDiseaseNameDiseaseMIMConceptIDSourceTypical associationHGMD variantsClinVar variantsHGNC IDGeneMIM
 
HPO disease - gene - phenotype typical associations:
 
HPO disease - gene - phenotype less frequent non-typical associations:
HP:0100799HP:0100799Neoplasm of the middle ear0VHL CL E G H7428892Billet Bear syndromeORPHA0135712687608537
HP:0100799HP:0100799Neoplasm of the middle ear0VHL CL E G H7428892Billet Bear syndromeORPHA0152412687608537
HP:0100799HP:0009797Cholesteatoma1VHL CL E G H7428892Billet Bear syndromeORPHA0152412687608537
HP:0100799HP:0009797Cholesteatoma1VHL CL E G H7428892Billet Bear syndromeORPHA0135712687608537


Genes (3) :EYA1 SIX1 VHL

Diseases (2) :892 113650
 

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