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Pachyonychia (NGS panel of 5 genes)
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Pachyonychia congenita (sequence analysis of KRT17 gene)
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Pachyonychia congenita (sequence analysis of KRT6A gene)
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Paget disease of bone (sequence analysis of TNFRSF11A gene)
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Palizaeus-Merzbacher-like disease (sequence analysis of GJC2 gene)
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Palmoplantar keratoderma and erythrokeratodermia (WES based NGS panel of 44 genes, including CNV analysis)
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Palmoplantar keratoderma, epidermolytic and non epidermolytic (sequence analysis of KRT1 gene)
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Palmoplantar keratoderma, epidermolytic (sequence analysis of KRT9 gene)
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Pancreatic agenesis (sequence analysis of PDX1 gene)
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Pancreatic agenesis 2 (sequence analysis of PTF1A gene)
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Pancreatic cancer (NGS panel for 5 genes, including CNV analysis)
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Pancreatic cancer, susceptibility (deletion/duplication analysis of PALB2 gene)
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Pancreatic cancer, susceptibility (sequence analysis of PALB2 gene)
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Pancreatic cancer, susceptibility to, 1 (P239S mutation on PALLD gene)
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Pancreatic cancer/melanoma syndrome (sequence analysis of CDKN2A gene)
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Pancreatic familial cancer, susceptibility to (sequence analysis of MADH4 gene)
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Pancreatic lipase deficiency (sequence analysis of PNLIP gene)
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Pancreatitis, chronic (N34S mutation on SPINK1 gene and R122H and N29I mutations on PRSS1 gene)
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Pancreatitis, chronic (sequence analysis of CTRC gene)
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Pancreatitis, hereditary (deletion/duplication analysis on PRSS1 and SPINK1 genes)
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