Human Phenotype Ontology 
Grandparent Node:
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Leukemia (HP:0001909)help
Parent Node:
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Acute leukemia (HP:0002488)help
..Starting node
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Acute monocytic leukemia (HP:0004845)help
Term ID: 4845
Name: Acute monocytic leukemia
Synonym: Acute monoblastic leukaemia; Acute monoblastic leukemia; Acute monocytic leukaemia; AML-M5; AMoL
Definition: The accumulation of transformed primitive hematopoietic blast cells, which lose their ability of normal differentiation and proliferation.
Comments:
Reference: HP:0004845
Genes and Diseases:
 
       Child Nodes:

 Sister Nodes: 
..expandAcute lymphoblastic leukemia (HP:0006721) help
..expandAcute megakaryocytic leukemia (HP:0006733) help
..expandAcute myeloid leukemia (HP:0004808) help
..expandAcute myelomonocytic leukemia (HP:0004820) help
..expandAcute promyelocytic leukemia (HP:0004836) help
..expandBiphenotypic acute leukemia (HP:0005531) 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:0004845HP:0004845Acute monocytic leukemia0ELANE CL E G H19913309OMIM:202700Neutropenia, severe congenital, 1, autosomal dominant.79
HP:0004845HP:0004845Acute monocytic leukemia0RUNX1 CL E G H86110471OMIM:601399Platelet disorder, familial, with associated myeloid malignancy.181
HP:0004845HP:0004845Acute monocytic leukemia0SPRED1 CL E G H16174220249ORPHA:137605Legius syndrome136


Genes (3) :ELANE RUNX1 SPRED1

Diseases (3) :OMIM:202700 OMIM:601399 ORPHA:137605
 

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