Human Phenotype Ontology 
Grandparent Node:
expand
Abnormality of the respiratory system (HP:0002086)help
Grandparent Node:
expand
Neoplasm by anatomical site (HP:0011793)help
Parent Node:
expand
Abnormal nasopharynx morphology (HP:0001739)help
Parent Node:
expand
Neoplasm of the respiratory system (HP:0100606)help
..Starting node
..expand
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; Tumour 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


Genes (5) :MST1R PDE11A PRKAR1A STK11 TP53

Diseases (4) :OMIM:617075 ORPHA:1359 ORPHA:2869 OMIM:607107
 

Human Phenotype Ontology(HPO) is developed by the Human Phenotype Ontology Consortium. The version used here is December 15 2022 release.