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 megakaryocytic leukemia (HP:0006733)help
Term ID: 6733
Name: Acute megakaryocytic leukemia
Synonym: Acute megakaryocytic leukaemia; AMegL
Definition: A rare subtype of acute myeloid leukemia evolving from primitive megakaryoblasts.
Comments:
Reference: HP:0006733
Genes and Diseases:
 
       Child Nodes:

 Sister Nodes: 
..expandAcute lymphoblastic leukemia (HP:0006721) help
..expandAcute monocytic leukemia (HP:0004845) 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:0006733HP:0006733Acute megakaryocytic leukemia0GATA1 CL E G H26234170OMIM:190685Down syndrometrisomy 21, included.29


Genes (1) :GATA1

Diseases (1) :OMIM:190685
 

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