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VACTERL association, X-linked (sequence analysis of ZIC3 gene)
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Van Buchem disease (sequence analysis of SOST gene)
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Van den Ende-Gupta syndrome (sequence analysis of SCARF2 gene)
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Van der Woude 2 syndrome (sequence analysis of do GRHL3 gene)
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Van Der Woude syndrome (deletion/duplication analysis on IRF6 gene)
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van der Woude syndrome | Popliteal pterygium syndrome (sequence analysis of IRF6 gene)
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Variant Rett Syndrome | Early infantile epileptic encephalopathy (sequence analysis of CDKL5 gene)
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VATERL association (sequence analysis of HOXD13 gene)
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Ventricular tachycardia, catecholaminergic polymorphic 1 (sequence analysis of RYR2 gene)
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Ventricular tachycardia, catecholaminergic polymorphic 4 (sequence analysis of CALM1 gene)
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Ventricular tachycardia, catecholaminergic polymorphic, 2 (sequence analysis of CASQ2 gene)
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Vesicoureteral reflux 2 (sequence analysis of ROBO2 gene)
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Vesicoureteral reflux 3 (sequence analysis of SOX17 gene)
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Vitamin B12 Deficiency (NGS panel of 20 genes)
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Vitamin D-dependent rickets type I (sequence analysis of CYP27B1 gene)
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Vitamin D-resistant rickets (sequence analysis of VDR gene)
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Vitamin K-dependent clotting factors, combined deficiency of, 1 | Pseudoxanthoma elasticum-like disorder with multiple coagulation factor deficiency (sequence analysis of GGCX gene)
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Vitiligo-associated multiple autoimmune disease susceptibility (sequence analysis of NLRP1 gene)
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Vitreoretinopathy (NGS panel of 27 genes)
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VLCAD deficiency (deletion/duplication on ACADVL gene)
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