| 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 |
| Similar Terms | |
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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 |
