Human Phenotype Ontology 
Grandparent Node:
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Abnormal nasopharynx morphology (HP:0001739)help
Grandparent Node:
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Neoplasm of the respiratory system (HP:0100606)help
Parent Node:
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Facial neoplasm (HP:0012289)help
Parent Node:
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Neoplasia of the nasopharynx (HP:0100630)help
..Starting node
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Neoplasm of the nose (HP:0012720)help
Term ID: 12720
Name: Neoplasm of the nose
Synonym: Nasal neoplasm; Nasal tumor; Nasal tumour; Neoplasia of the nose; Nose cancer; Tumor of the nose; Tumour of the nose
Definition: Tumor (An abnormal mass of tissue resulting from abnormally dividing cells) of the nasal cavity.
Comments:
Reference: HP:0012720
Genes and Diseases:
 
       Child Nodes:
........expandParanasal sinus neoplasm (HP:0030072) help

 Sister Nodes: 
..expandNeoplasm of the pharynx (HP:0100638) 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:0012720HP:0012720Neoplasm of the nose0STK11 CL E G H67942869Hypertrophic osteoarthropathy, primary or idiopathicORPHA0182011389602216
HP:0012720HP:0012720Neoplasm of the nose0STK11 CL E G H67942869Hypertrophic osteoarthropathy, primary or idiopathicORPHA0194511389602216
HP:0012720HP:0030072Paranasal sinus neoplasm1STK11 CL E G H67942869Hypertrophic osteoarthropathy, primary or idiopathicORPHA0194511389602216
HP:0012720HP:0030072Paranasal sinus neoplasm1STK11 CL E G H67942869Hypertrophic osteoarthropathy, primary or idiopathicORPHA0182011389602216


Genes (1) :STK11

Diseases (1) :2869
 

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