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 larynx (HP:0001600)help
Parent Node:
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Neoplasm of the respiratory system (HP:0100606)help
..Starting node
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Neoplasm of the larynx (HP:0100605)help
Term ID: 100605
Name: Neoplasm of the larynx
Synonym:
Definition:
Comments:
Reference: HP:0100605
Genes and Diseases:
 
       Child Nodes:
........expandLaryngeal carcinoma (HP:0012118) help

 Sister Nodes: 
..expandNeoplasia of the nasopharynx (HP:0100630) help
..expandNeoplasia of the pleura (HP:0100527) help
..expandNeoplasm of the lung (HP:0100526) 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:0100605HP:0100605Neoplasm of the larynx0 CL E G H
HP:0100605HP:0100605Neoplasm of the larynx1 CL E G H


Genes (4) :MLH1 MSH2 MSH6 RSPO1

Diseases (3) :587 158320 610644
 

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