anemia, hypochromic microcytic Gene Set

Dataset OMIM Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
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1 genes associated with the anemia, hypochromic microcytic phenotype from the curated OMIM Gene-Disease Associations dataset.

Symbol Name
SLC11A2 solute carrier family 11 (proton-coupled divalent metal ion transporter), member 2