|Dataset||OMIM Gene-Disease Associations|
|Category||disease or phenotype associations|
|Description||Thiamine-responsive megaloblastic anemia (TRMA) is characterized by a triad of megaloblastic anemia, non-type I diabetes mellitus, and sensorineural deafness. (Orphanet Rare Disease Ontology, Orphanet_49827)|
|Downloads & Tools|
1 genes associated with the thiamine-responsive megaloblastic anemia syndrome phenotype from the curated OMIM Gene-Disease Associations dataset.
|SLC19A2||solute carrier family 19 (thiamine transporter), member 2|