hypochromic microcytic anemia Gene Set

Dataset HPO 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)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0004840
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Genes

8 genes associated with the hypochromic microcytic anemia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
ABCB7 ATP-binding cassette, sub-family B (MDR/TAP), member 7
ALAS2 5'-aminolevulinate synthase 2
ATRX alpha thalassemia/mental retardation syndrome X-linked
HBA1 hemoglobin, alpha 1
HBA2 hemoglobin, alpha 2
HBB hemoglobin, beta
LCRB locus control region, beta
TMPRSS6 transmembrane protease, serine 6