Chronic Hemolytic Anemia Gene Set

Dataset DisGeNET Gene-Disease Associations
Category disease or phenotype associations
Type disease
Description An chronic form of hemolytic anemia. (Human Phenotype Ontology, HP_0004870)
External Link https://www.disgenet.org/browser/0/1/0/C1387532
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Genes

15 genes associated with the disease Chronic Hemolytic Anemia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Symbol Name
ABCG5 ATP-binding cassette, sub-family G (WHITE), member 5
ABCG8 ATP-binding cassette, sub-family G (WHITE), member 8
AK1 adenylate kinase 1
CGA glycoprotein hormones, alpha polypeptide
G6PD glucose-6-phosphate dehydrogenase
GPI glucose-6-phosphate isomerase
HAMP hepcidin antimicrobial peptide
HBA1 hemoglobin, alpha 1
HBA2 hemoglobin, alpha 2
HBB hemoglobin, beta
KCNN4 potassium channel, calcium activated intermediate/small conductance subfamily N alpha, member 4
NHLRC2 NHL repeat containing 2
PKLR pyruvate kinase, liver and RBC
TPI1 triosephosphate isomerase 1
UBL4A ubiquitin-like 4A