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Haim-Munk syndrome | Papillon-Lefevre syndrome | Periodontitis 1, juvenile (deletion/duplication analysis of CTSC gene)
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Hamamy syndrome (sequence analysis of IRX5 gene)
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Hartnup disorder (sequence analysis of SLC6A19 gene)
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Hawkinsinuria (sequence analysis of HPD gene)
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Helsmoortel-van der Aa syndrome (sequence analysis of ADNP gene)
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Hemiplegic familial migraine (deletion/duplication analysis on CACNA1A gene)
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Hemiplegic familial migraine (deletion/duplication analysis on SCN1A gene)
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Hemiplegic familial migraine (NGS panel of 3 genes)
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Hemochromatosis (NGS panel for 8 genes)
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Hemochromatosis (sequence analysis of HFE gene)
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Hemochromatosis type 2A (sequence analysis of HFE2/HJV gene)
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Hemochromatosis type 2B (sequence analysis of HAMP gene)
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Hemochromatosis type 3 (sequence analysis of TFR2 gene)
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Hemochromatosis type 4 (sequence analysis of SLC40A1 gene)
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Hemochromatosis type 5 (sequence analysis of FTH1 gene)
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Hemolytic anemia (NGS panel of 33 genes)
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Hemolytic anemia due to adenylate kinase deficiency (sequence analysis of AK1 gene)
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Hemolytic anemia due to glucophosphate isomerase deficiency (sequence analysis of GPI gene)
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Hemolytic anemia due to glutathione reductase deficiency (sequence analysis of GSR gene)
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Hemolytic anemia due to pyrimidine 5' nucleotidase deficiency (sequence analysis of NT5C3A gene)
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