thiamine-responsive megaloblastic anemia syndrome Gene Set

Dataset OMIM Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
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)
External Link http://www.omim.org/entry/249270
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Genes

1 genes associated with the thiamine-responsive megaloblastic anemia syndrome phenotype from the curated OMIM Gene-Disease Associations dataset.

Symbol Name
SLC19A2 solute carrier family 19 (thiamine transporter), member 2