Human Phenotype Ontology 
Grandparent Node:
expandAcute leukemia (HP:0002488)help
Parent Node:
expandAcute lymphoblastic leukemia (HP:0006721)help
..Starting node
..expandT-cell acute lymphoblastic leukemias (HP:0006727)help
Term ID: 6727
Name: T-cell acute lymphoblastic leukemias
Synonym:
Definition: Acute lymphoblastic leukemia of T-cell origin. It comprises about 15% of childhood cases and 25% of adult cases. It is more common in males than females.
Comments:
Reference: HP:0006727
Genes and Diseases:
 
       Child Nodes:

 Sister Nodes: 
..expandB Acute Lymphoblastic Leukemia (HP:0004812) help
..expandPh-positive acute lymphoblastic leukemia (HP:0004848) 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:0006727HP:0006727T-cell acute lymphoblastic leukemias0BRCA2 CL E G H6751101OMIM:605724Fanconi anemia, complementation group D17642
HP:0006727HP:0006727T-cell acute lymphoblastic leukemias0DUT CL E G H18543078OMIM:620044
HP:0006727HP:0006727T-cell acute lymphoblastic leukemias0MSH2 CL E G H44367325OMIM:619096MISMATCH REPAIR CANCER SYNDROME 2; MMRCS22162


Genes (3) :BRCA2 DUT MSH2

Diseases (3) :OMIM:605724 OMIM:620044 OMIM:619096
 

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