Thiamine-responsive Megaloblastic Anemia Syndrome
Description
Thiamine-responsive megaloblastic anemia (TRMA) is characterized by a triad of megaloblastic anemia, non-type I diabetes mellitus, and sensorineural deafness.
Genes related to Thiamine-responsive Megaloblastic Anemia Syndrome
- SLC19A2
Clinical Features
Top most frequent phenotypes and symptoms related to Thiamine-responsive Megaloblastic Anemia Syndrome
- Seizures
- Global developmental delay
- Short stature
- Hearing impairment
- Microcephaly
- Ataxia
- Nystagmus
- Sensorineural hearing impairment
- Cryptorchidism
- Anemia
And another 46 symptoms. If you need more information about this disease we can help you.
Incidence and onset information
— Currently we don't have prevalence information about this disease (Not enough data available about incidence and published cases.)— No data available about the known clinical features onset.
Alternative names
Thiamine-responsive Megaloblastic Anemia Syndrome Is also known as thmd1, trma, thiamine-responsive megaloblastic anemia with diabetes mellitus and sensorineural deafness, rogers syndrome, thiamine-responsive myelodysplasia, thiamine metabolism dysfunction syndrome 1 (megaloblastic anemia, diabetes mellitus, and deafness type.
Researches and researchers
Currently, we don't have any information about doctors, researches or researchers related to this disease. Please contact us if you would like to appear here.Thiamine-responsive Megaloblastic Anemia Syndrome Recommended genes panels
Panel Name, Specifity and genes Tested/covered |
---|
![]() By Athena Diagnostics Inc (United States).
BCS1L, ROR1, SALL1, SEMA3E, SIX1, SIX5, SLC12A1, SLC19A2, SLC22A4, SNAI2, SMPX, SOX10, TBX1, TCOF1, TECTA, TFAP2A, TIMM8A, TJP2, TMPRSS3, USH1C , (...)
View the complete list with 149 more genes
Specificity
1 %
Genes
100 % |
![]() By Clinical Molecular Genetics Laboratory Johns Hopkins All Children's Hospital (United States).
SLC19A2
Specificity
100 %
Genes
100 % |
![]() By Knight Diagnostic Laboratories - Molecular Diagnostic Center Oregon Health & Science University (United States).
RPS6KA3, SALL1, SEMA3E, SIX1, SIX5, SLC19A2, SNAI2, SMPX, SOX10, BTD, TCOF1, TECTA, TIMM8A, TJP2, TMPRSS3, USH1C, USH2A, CLRN1, WFS1, ESPN , (...)
View the complete list with 100 more genes
Specificity
1 %
Genes
100 % |
![]() By Genetic Services Laboratory University of Chicago (United States).
SLC19A2
Specificity
100 %
Genes
100 % |
![]() By Genetic Services Laboratory University of Chicago (United States).
SLC19A2
Specificity
100 %
Genes
100 % |
![]() By Genetic Services Laboratory University of Chicago (United States).
BCS1L, RTN2, SACS, SCN1A, SCN2A, SCN8A, SCO1, SDHA, SDHD, SLC16A2, SLC17A5, SLC19A2, SLC1A3, SLC20A2, SLC2A1, SLC6A1, SLC9A1, SLC9A6, SNAP25, SOD1 , (...)
View the complete list with 457 more genes
Specificity
1 %
Genes
100 % |
![]() By Instituto de Medicina Genomica Instituto de Medicina Genomica (Spain).
SLC19A2
Specificity
100 %
Genes
100 % |
![]() By CGC Genetics (Portugal).
SLC19A2
Specificity
100 %
Genes
100 % |
You can get up to 34 more panels with our dedicated tool
Learn moreSources and references
You can check the following sources for additional information.
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