Thiamine responsive megaloblastic anemia syndrome Gene Set

Dataset CTD Gene-Disease Associations
Category disease or phenotype associations
Type disease
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://ctdbase.org/detail.go?type=disease&acc=MESH:C536510
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Genes

1 genes/proteins associated with the disease Thiamine responsive megaloblastic anemia syndrome from the curated CTD Gene-Disease Associations dataset.

Symbol Name Standardized Value
SLC19A2 solute carrier family 19 (thiamine transporter), member 2 2.88009