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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Lymphoproliferative disorder (HP:0005523)help
Term ID: 5523
Name: Lymphoproliferative disorder
Synonym: Lymphoproliferative disorders
Definition:
Comments:
Reference: HP:0005523
Genes and Diseases:
 
       Child Nodes:
........expandMonoclonal immunoglobulin M proteinemia (HP:0005508) help

 Sister Nodes: 
..expandLeukemia (HP:0001909) help
..expandLymphoma (HP:0002665) help
..expandMalignant eosinophil proliferation (HP:0006782) 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:0005523HP:0005523Lymphoproliferative disorder0CD70 CL E G H970618261618261618261OMIM1411937602840
HP:0005523HP:0005523Lymphoproliferative disorder0KRAS CL E G H3845614470RAS-associated autoimmune leukoproliferative disorder614470C2674723OMIM1456407190070
HP:0005523HP:0005523Lymphoproliferative disorder0MCM4 CL E G H4173609981Natural killer cell and glucocorticoid deficiency with DNA repair defect609981C1864947OMIM156947602638
HP:0005523HP:0005523Lymphoproliferative disorder0NRAS CL E G H4893614470RAS-associated autoimmune leukoproliferative disorder614470C2674723OMIM1147989164790
HP:0005523HP:0005523Lymphoproliferative disorder1CD70 CL E G H970618261618261618261OMIM1411937602840
HP:0005523HP:0005523Lymphoproliferative disorder1KRAS CL E G H3845614470RAS-associated autoimmune leukoproliferative disorder614470C2674723OMIM1456407190070
HP:0005523HP:0005523Lymphoproliferative disorder1MCM4 CL E G H4173609981Natural killer cell and glucocorticoid deficiency with DNA repair defect609981C1864947OMIM156947602638
HP:0005523HP:0005523Lymphoproliferative disorder1NRAS CL E G H4893614470RAS-associated autoimmune leukoproliferative disorder614470C2674723OMIM1147989164790
 
HPO disease - gene - phenotype less frequent non-typical associations:
HP:0005523HP:0005523Lymphoproliferative disorder0CD27 CL E G H939615122Lymphoproliferative syndrome 2615122C3554540OMIM0811922186711
HP:0005523HP:0005523Lymphoproliferative disorder1CD27 CL E G H939615122Lymphoproliferative syndrome 2615122C3554540OMIM0811922186711


Genes (6) :CD27 CD70 KRAS MCM4 MYD88 NRAS

Diseases (6) :615122 618261 614470 609981 33226 153600
 

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