Search Ontology:
Human Disease
thiamine-responsive megaloblastic anemia syndrome
- Term ID
- DOID:0090117
- Synonyms
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- Rogers syndrome
- thiamine metabolism dysfunction syndrome 1
- thiamine-responsive anaemia syndrome
- thiamine-responsive anemia syndrome
- thiamine-responsive megaloblastic anaemia syndrome
- thiamine-responsive megaloblastic anaemia with diabetes mellitus and sensorineural deafness
- thiamine-responsive megaloblastic anemia with diabetes mellitus and sensorineural deafness
- thiamine-responsive myelodysplasia
- THMD1
- TRMA
- Definition
- A syndrome 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. (3)
- References
-
- GARD:9210
- MESH:C536510
- MIM:249270
- ORDO:498277
- SNOMEDCT_US_2023_03_01:237617006
- UMLS_CUI:C0342287
- Ontology
- Human Disease ( DOID:0090117 )
- is a type of
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Genes Involved
Zebrafish Models