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15 Possible Causes for XK 46

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  • Glycogen Storage Disease due to Phosphoglycerate Kinase 1 Deficiency

    ) Next Generation Sequencing (NGS) of coding exons and flanking sequences (‘splice sites’) of 46 genes causing hereditary hemolytic anemia.[umcutrecht.nl] GCLC, GPI, GPX1, GSR, GSS, HBA1, HBA2, HBB, HK1, KCNN4, KIF23, KLF1, NT5C3A, PFKM, PGD, PGK1, PGLS, PIEZO1, PKLR, RHAG, SEC23B, SLC2A1, SLC4A1, SPTA1, SPTB, TALDO1, TPI1, XK[umcutrecht.nl]

  • Autosomal Dominant Secondary Polycythemia

    ) Next Generation Sequencing (NGS) of coding exons and flanking sequences (‘splice sites’) of 46 genes causing hereditary hemolytic anemia.[umcutrecht.nl] GCLC, GPI, GPX1, GSR, GSS, HBA1, HBA2, HBB, HK1, KCNN4, KIF23, KLF1, NT5C3A, PFKM, PGD, PGK1, PGLS, PIEZO1, PKLR, RHAG, SEC23B, SLC2A1, SLC4A1, SPTA1, SPTB, TALDO1, TPI1, XK[umcutrecht.nl]

  • Acute Hemolytic Anemia

    ) Next Generation Sequencing (NGS) of coding exons and flanking sequences (‘splice sites’) of 46 genes causing hereditary hemolytic anemia.[umcutrecht.nl] GCLC, GPI, GPX1, GSR, GSS, HBA1, HBA2, HBB, HK1, KCNN4, KIF23, KLF1, NT5C3A, PFKM, PGD, PGK1, PGLS, PIEZO1, PKLR, RHAG, SEC23B, SLC2A1, SLC4A1, SPTA1, SPTB, TALDO1, TPI1, XK[umcutrecht.nl]

  • Anemia due to Glutathione Metabolism Disorder

    ) Next Generation Sequencing (NGS) of coding exons and flanking sequences (‘splice sites’) of 46 genes causing hereditary hemolytic anemia.[umcutrecht.nl] GCLC, GPI, GPX1, GSR, GSS, HBA1, HBA2, HBB, HK1, KCNN4, KIF23, KLF1, NT5C3A, PFKM, PGD, PGK1, PGLS, PIEZO1, PKLR, RHAG, SEC23B, SLC2A1, SLC4A1, SPTA1, SPTB, TALDO1, TPI1, XK[umcutrecht.nl]

  • Pyrimidine-5-Nucleotidase Deficiency

    ) Next Generation Sequencing (NGS) of coding exons and flanking sequences (‘splice sites’) of 46 genes causing hereditary hemolytic anemia.[umcutrecht.nl] GCLC, GPI, GPX1, GSR, GSS, HBA1, HBA2, HBB, HK1, KCNN4, KIF23, KLF1, NT5C3A, PFKM, PGD, PGK1, PGLS, PIEZO1, PKLR, RHAG, SEC23B, SLC2A1, SLC4A1, SPTA1, SPTB, TALDO1, TPI1, XK[umcutrecht.nl]

  • Familial Atrial Fibrillation 6

    View Article : Google Scholar : PubMed/NCBI 46 Olson TM, Alekseev AE, Liu XK, Park S, Zingman LV, Bienengraeber M, Sattiraju S, Ballew JD, Jahangir A and Terzic A: Kv1.5 channelopathy[spandidos-publications.com]

  • Congenital Hemolytic Anemia

    ) Next Generation Sequencing (NGS) of coding exons and flanking sequences (‘splice sites’) of 46 genes causing hereditary hemolytic anemia.[umcutrecht.nl] GCLC, GPI, GPX1, GSR, GSS, HBA1, HBA2, HBB, HK1, KCNN4, KIF23, KLF1, NT5C3A, PFKM, PGD, PGK1, PGLS, PIEZO1, PKLR, RHAG, SEC23B, SLC2A1, SLC4A1, SPTA1, SPTB, TALDO1, TPI1, XK[umcutrecht.nl]

  • Phosphoglycerate Kinase Deficiency

    ) Next Generation Sequencing (NGS) of coding exons and flanking sequences (‘splice sites’) of 46 genes causing hereditary hemolytic anemia.[umcutrecht.nl] GCLC, GPI, GPX1, GSR, GSS, HBA1, HBA2, HBB, HK1, KCNN4, KIF23, KLF1, NT5C3A, PFKM, PGD, PGK1, PGLS, PIEZO1, PKLR, RHAG, SEC23B, SLC2A1, SLC4A1, SPTA1, SPTB, TALDO1, TPI1, XK[umcutrecht.nl]

  • Hereditary Pyropoikilocytosis

    ) Next Generation Sequencing (NGS) of coding exons and flanking sequences (‘splice sites’) of 46 genes causing hereditary hemolytic anemia.[umcutrecht.nl] GCLC, GPI, GPX1, GSR, GSS, HBA1, HBA2, HBB, HK1, KCNN4, KIF23, KLF1, NT5C3A, PFKM, PGD, PGK1, PGLS, PIEZO1, PKLR, RHAG, SEC23B, SLC2A1, SLC4A1, SPTA1, SPTB, TALDO1, TPI1, XK[umcutrecht.nl]

  • Hexokinase Deficiency

    ) Next Generation Sequencing (NGS) of coding exons and flanking sequences (‘splice sites’) of 46 genes causing hereditary hemolytic anemia.[umcutrecht.nl] GCLC, GPI, GPX1, GSR, GSS, HBA1, HBA2, HBB, HK1, KCNN4, KIF23, KLF1, NT5C3A, PFKM, PGD, PGK1, PGLS, PIEZO1, PKLR, RHAG, SEC23B, SLC2A1, SLC4A1, SPTA1, SPTB, TALDO1, TPI1, XK[umcutrecht.nl]

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