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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Abnormal pleura morphology (HP:0002103)help
Parent Node:
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Neoplasm of the respiratory system (HP:0100606)help
..Starting node
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Neoplasia of the pleura (HP:0100527)help
Term ID: 100527
Name: Neoplasia of the pleura
Synonym:
Definition:
Comments:
Reference: HP:0100527
Genes and Diseases:
 
       Child Nodes:
........expandPleural mesothelioma (HP:0100002) help
........expandPleuropulmonary blastoma (HP:0100528) help

 Sister Nodes: 
..expandNeoplasia of the nasopharynx (HP:0100630) 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:
 
HPO disease - gene - phenotype less frequent non-typical associations:
HP:0100527HP:0100527Neoplasia of the pleura0 CL E G H
HP:0100527HP:0100528Pleuropulmonary blastoma1 CL E G H
HP:0100527HP:0100002Pleural mesothelioma1 CL E G H


Genes (2) :DICER1 KEAP1

Diseases (3) :276399 601200 180295
 

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