|Dataset||GAD Gene-Disease Associations|
|Category||disease or phenotype associations|
|Description||A type of chromosomal aberration characterized by an increased susceptibility to chromosomal breakage induced by treatment of cultured lymphocytes with agents such as chemical mutagens, irradiation, and alkylating agents. (Human Phenotype Ontology, HP_0003220)|
|Downloads & Tools|
2 genes associated with the disease chromosome breakage in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.