erythroid hyperplasia Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description Increased count of erythroid precursor cells, that is, erythroid lineage cells in the bone marrow. (Human Phenotype Ontology, HP_0012132)
External Link
Similar Terms
Downloads & Tools


5 genes associated with the erythroid hyperplasia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
C15ORF41 chromosome 15 open reading frame 41
CDAN1 codanin 1
GIF gastric intrinsic factor (vitamin B synthesis)
KLF1 Kruppel-like factor 1 (erythroid)
PUS1 pseudouridylate synthase 1