hypochromic microcytic anemia Gene Set

Dataset OMIM Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description A microcytic anemia characterized by paler than normal blood cells. (Human Disease Ontology, DOID_0050642)
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Genes

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

Symbol Name
HBA2 hemoglobin, alpha 2