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Disease Ontology Browser
thiamine-responsive megaloblastic anemia syndrome (DOID:0090117)
Alliance: disease page
Synonyms: Rogers syndrome; thiamine metabolism dysfunction syndrome 1; thiamine-responsive anemia syndrome; thiamine-responsive megaloblastic anemia with diabetes mellitus and sensorineural deafness; thiamine-responsive myelodysplasia; THMD1; TRMA
Alt IDs: OMIM:249270, MESH:C536510, ORDO:498277, UMLS_CUI:C0342287
Definition: An autosomal recessive disease that is characterized by megaloblastic anemia, non-type I diabetes mellitus, and sensorineural deafness where the anemia and sometimes diabetes is repsonsive to high doses of thiamine, and that has_material_basis_in homozygous mutation in the solute carrier family 19 member 2 (SLC19A2) gene on chromosome 1q24.

Disease References using Mouse Models (2)

Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB), Gene Ontology (GO)
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last database update
02/18/2020
MGI 6.14
The Jackson Laboratory