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t(11;14)(IGH/BCL1) rearrangement
+ info
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t(14;18)(IGH/BCL2) rearrangement
+ info
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T-B+ severe combined immunodeficiency due to CD45 deficiency (sequence analysis of PTPRC gene)
+ info
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T-B+ severe combined immunodeficiency due to IL-7Ralpha deficiency (deletion/duplication analysis of IL7R gene)
+ info
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T-B+ severe combined immunodeficiency due to IL-7Ralpha deficiency (sequence analysis of IL7R gene)
+ info
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T-cell immunodeficiency, congenital alopecia, and nail dystrophy (sequence analysis of FOXN1 gene)
+ info
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T21, T18, T13 only
+ info
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Tamoxifen pharmacogenetics
+ info
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Tangier disease (sequence analysis of ABCA1 gene)
+ info
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Tatton-Brown-Rahman syndrome (sequence analysis of DNMT3A gene)
+ info
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Tay-Sachs disease (deletion/duplication analysis of HEXA gene)
+ info
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Tay-Sachs disease (sequence analysis of HEXA gene)
+ info
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TCRB clonal rearrangement
+ info
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TCRD clonal rearrangement
+ info
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TCRG clonal rearrangement
+ info
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Temtamy syndrome (sequence analysis of C12ORF57 gene)
+ info
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Tetra-amelia AR (sequence analysis of WNT3 gene)
+ info
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Thiamine metabolism dysfunction syndrome 4 progressive polyneuropathy type (sequence analysis of SLC25A19 gene)
+ info
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Thiamine metabolism dysfunction syndrome 5 (episodic encephalopathy type) (deletion/duplication analysis of TPK1 gene)
+ info
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Thiamine-responsive megaloblastic anemia syndrome (sequence analysis of SLC19A2 gene)
+ info
