Human Phenotype Ontology 
Grandparent Node:
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Abnormality of blood and blood-forming tissues (HP:0001871)help
Grandparent Node:
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Neoplasm by anatomical site (HP:0011793)help
Parent Node:
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Hematological neoplasm (HP:0004377)help
..Starting node
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Malignant eosinophil proliferation (HP:0006782)help
Term ID: 6782
Name: Malignant eosinophil proliferation
Synonym:
Definition:
Comments:
Reference: HP:0006782
Genes and Diseases:
 
       Child Nodes:

 Sister Nodes: 
..expandLeukemia (HP:0001909) help
..expandLymphoma (HP:0002665) help
..expandLymphoproliferative disorder (HP:0005523) help
..expandMultiple myeloma (HP:0006775) help
..expandMyelodysplasia (HP:0002863) help
..expandPlasmacytoma (HP:0011857) help
InputHPO IDHPO termDistanceGeneGene id entrezDiseaseIdDiseaseNameDiseaseMIMConceptIDSourceTypical associationHGMD variantsClinVar variantsHGNC IDGeneMIM
 
HPO disease - gene - phenotype typical associations:
HP:0006782HP:0006782Malignant eosinophil proliferation0PDGFRB CL E G H5159131440Malignant eosinophil proliferation131440C1851585OMIM1248804173410
 
HPO disease - gene - phenotype less frequent non-typical associations:


Genes (1) :PDGFRB

Diseases (1) :131440
 

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