|Dataset||OMIM Gene-Disease Associations|
|Category||disease or phenotype associations|
|Description||Anemia characterized by abnormal intracellular inclusions, composed of denatured hemoglobin, found on the membrane of red blood cells. (Human Phenotype Ontology, HP_0005511)|
|Downloads & Tools|
1 genes associated with the heinz body anemia phenotype from the curated OMIM Gene-Disease Associations dataset.
|HBA2||hemoglobin, alpha 2|