Human Phenotype Ontology 
Grandparent Node:
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Leukemia (HP:0001909)help
Parent Node:
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Chronic leukemia (HP:0005558)help
..Starting node
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Chronic myelogenous leukemia (HP:0005506)help
Term ID: 5506
Name: Chronic myelogenous leukemia
Synonym: Chronic myelocytic leukaemia; Chronic myelocytic leukemia; Chronic myelogenous leukaemia; Chronic myeloid leukaemia; Chronic myeloid leukemia
Definition: A myeloproliferative disorder characterized by increased proliferation of the granulocytic cell line without the loss of their capacity to differentiate.
Comments:
Reference: HP:0005506
Genes and Diseases:
 
       Child Nodes:

 Sister Nodes: 
..expandChronic lymphatic leukemia (HP:0005550) help
InputHPO IDHPO termDistanceGeneGene id entrezHGNC IDDiseaseIdDiseaseNameFrequencyOnsetHGMD variantsClinVar variants
 
HPO disease - gene - phenotype typical associations:
 
HPO disease - gene - phenotype less frequent non-typical associations:
HP:0005506HP:0005506Chronic myelogenous leukemia0ABL1 CL E G H2576OMIM:608232Leukemia, chronic myeloid.51
HP:0005506HP:0005506Chronic myelogenous leukemia0BCR CL E G H6131014OMIM:608232Leukemia, chronic myeloid.5
HP:0005506HP:0005506Chronic myelogenous leukemia0JAK2 CL E G H37176192ORPHA:71493Familial thrombocytosisHP:0040283 - Occasional57
HP:0005506HP:0005506Chronic myelogenous leukemia0MPL CL E G H43527217ORPHA:71493Familial thrombocytosisHP:0040283 - Occasional97
HP:0005506HP:0005506Chronic myelogenous leukemia0THPO CL E G H706611795ORPHA:71493Familial thrombocytosisHP:0040283 - Occasional23


Genes (5) :ABL1 BCR JAK2 MPL THPO

Diseases (2) :OMIM:608232 ORPHA:71493
 

Human Phenotype Ontology(HPO) is developed by the Human Phenotype Ontology Consortium. The version used here is December 15 2022 release.