Human Phenotype Ontology 
Grandparent Node:
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Abnormality of the respiratory system (HP:0002086)help
Grandparent Node:
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Neoplasm by anatomical site (HP:0011793)help
Parent Node:
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Abnormality of the nasopharynx (HP:0001739)help
Parent Node:
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Neoplasm of the respiratory system (HP:0100606)help
..Starting node
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Neoplasia of the nasopharynx (HP:0100630)help
Term ID: 100630
Name: Neoplasia of the nasopharynx
Synonym: Nasopharyngeal neoplasm; Neoplasm of the nasopharynx; Tumor of the nasopharynx
Definition:
Comments:
Reference: HP:0100630
Genes and Diseases:
 
       Child Nodes:
........expandNeoplasm of the nose (HP:0012720) help
................... HP:0030072 Paranasal sinus neoplasm
........expandNeoplasm of the pharynx (HP:0100638) help

 Sister Nodes: 
..expandNeoplasia of the pleura (HP:0100527) help
..expandNeoplasm of the larynx (HP:0100605) help
..expandNeoplasm of the lung (HP:0100526) help
InputHPO IDHPO termDistanceGeneGene id entrezDiseaseIdDiseaseNameDiseaseMIMConceptIDSourceTypical associationHGMD variantsClinVar variantsHGNC IDGeneMIM
 
HPO disease - gene - phenotype typical associations:
HP:0100630HP:0100630Neoplasia of the nasopharynx0TP53 CL E G H7157607107Nasopharyngeal carcinoma607107C2931822OMIM154111998191170
HP:0100630HP:0100630Neoplasia of the nasopharynx1TP53 CL E G H7157607107Nasopharyngeal carcinoma607107C2931822OMIM154111998191170
HP:0100630HP:0100630Neoplasia of the nasopharynx2TP53 CL E G H7157607107Nasopharyngeal carcinoma607107C2931822OMIM154111998191170
 
HPO disease - gene - phenotype less frequent non-typical associations:


Genes (2) :STK11 TP53

Diseases (2) :607107 2869
 

Human Phenotype Ontology(HPO) is developed by the Human Phenotype Ontology Consortium. The version used here is June 2019 release.