heinz body anemia Gene Set

Dataset OMIM Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description Anemia characterized by abnormal intracellular inclusions, composed of denatured hemoglobin, found on the membrane of red blood cells. (Human Phenotype Ontology, HP_0005511)
External Link http://www.omim.org/entry/140700
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Genes

1 genes associated with the heinz body anemia phenotype from the curated OMIM Gene-Disease Associations dataset.

Symbol Name
HBA2 hemoglobin, alpha 2