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Pseudohypoparathyroidism type 1A, 1B, 1C | Pseudopseudohypoparathyroidism | Osseous heteroplasia, progressive | Albright hereditary osteodystrophy (methylation and deletion/duplication analysis on GNAS gene)
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Pseudohypoparathyroidism type 1B (deletion/duplication analysis on STX16 gene)
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Pseudohypoparathyroidism type 1B (sequence analysis of STX16 gene)
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Pseudoxanthoma elasticum (deletion/duplication analysis on ABCC6 gene)
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Pseudoxanthoma elasticum (sequence analysis of ABCC6 gene)
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Pseudoxanthoma elasticum (sequence analysis of exons 24 and 28 of ABCC6 gene)
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Psoriasis 2 (sequence analysis of CARD14 gene)
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Psoriasis, generalized pustular (sequence analysis of IL36RN gene)
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Psychomotor development delay (various syndromes, deletion/duplication analysis)
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Pulmonary fibrosis and/or bone marrow failure (sequence analysis of TERT gene)
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Pulmonary fibrosis, family (NGS panel of 71 genes)
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Pulmonary fibrosis, idiopathic (sequence analysis of SFTPA1 gene)
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Pulmonary hypertension, primary (NGS panel for 9 genes)
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Pulmonary hypertension, primary, 2 (sequence analysis of SMAD9 gene)
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Pulmonary hypertension, primary, 4 (sequence analysis of KCNK3 gene)
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Pulmonary surfactant metabolism dysfunction (deletion/duplication analysis of ABCA3 gene)
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Pulmonary surfactant metabolism dysfunction (NGS panel of 7 genes)
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Pulmonary surfactant metabolism dysfunction (sequence analysis of ABCA3 gene)
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Pulmonary surfactant metabolism dysfunction 1 (sequence analysis of SFTPB gene)
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Pulmonary venoocclusive disease 2 (sequence analysis of EIF2AK4 gene)
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