thiamine-responsive megaloblastic anemia syndrome

Summary
Synonym
  • Rogers syndrome
  • THMD1
  • TRMA
  • 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
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.
Super Class
autosomal recessive disease syndrome
Disease Ontology
DOID:0090117
Mondo Disease Ontology
MeSH
UMLS
ORDO
OMIM
GARD
MGI genotype (from TogoID)
Related Genes
Displaying 1 entry
Gene ID Gene Symbol Description Source
10560 SLC19A2 solute carrier family 19 member 2
Displaying 1 entry
Gene ID Gene Symbol Description Source
116914 Slc19a2 solute carrier family 19 (thiamine transporter), member 2
Displaying all 3 entries
Gene ID Gene Symbol Description Source
178745 folt-2 Folate-like transporter 2
179544 folt-1 Folate transporter 1
4363081 folt-3 Folate-like transporter 3

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Acknowledgements

Supported by JST NBDC Grant Number JPMJND2204

Partly supported by NIH Common Fund Grant #1U01GM125267-01


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Last updated: December 9, 2024