congenital dyserythropoietic anemia Gene Set

Dataset DISEASES Curated Gene-Disease Assocation Evidence Scores
Category disease or phenotype associations
Type disease
Description A congenital hemolytic anemia characterized by ineffective erythropoiesis, and resulting from a decrease in the number of red blood cells (RBCs) in the body and a less than normal quantity of hemoglobin in the blood. (Human Disease Ontology, DOID_1338)
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Genes

5 genes involed in the disease congenital dyserythropoietic anemia from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.

Symbol Name
CDAN1 codanin 1
HBB hemoglobin, beta
KLF1 Kruppel-like factor 1 (erythroid)
LPIN2 lipin 2
SEC23B Sec23 homolog B (S. cerevisiae)