Thiamine-Responsive Megaloblastic Anemia Gene Set

Dataset DisGeNET Gene-Disease Associations
Category disease or phenotype associations
Type disease
Description A type of megaloblastic anemia (i.e., anemia characterized by the presence of erythroblasts that are larger than normal) that improves upon the administration of thiamine. (Human Phenotype Ontology, HP_0004860)
External Link https://www.disgenet.org/browser/0/1/0/C0271972
Similar Terms
Downloads & Tools

Genes

4 genes associated with the disease Thiamine-Responsive Megaloblastic Anemia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Symbol Name
ALMS1 Alstrom syndrome protein 1
CISD2 CDGSH iron sulfur domain 2
SLC19A2 solute carrier family 19 (thiamine transporter), member 2
WFS1 Wolfram syndrome 1 (wolframin)