Gene | Disease | Score gda | Association Type | Original DB | Sentence supporting the association | PMID | PMID Year | ||||||||
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0.700 | Biomarker | GENOMICS_ENGLAND | |||||||||||
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0.490 | Biomarker | GENOMICS_ENGLAND | |||||||||||
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0.470 | Biomarker | GENOMICS_ENGLAND | |||||||||||
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0.420 | Biomarker | GENOMICS_ENGLAND | |||||||||||
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0.410 | Biomarker | GENOMICS_ENGLAND | |||||||||||
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0.410 | Biomarker | GENOMICS_ENGLAND | |||||||||||
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0.410 | Biomarker | GENOMICS_ENGLAND | |||||||||||
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0.400 | Biomarker | GENOMICS_ENGLAND | |||||||||||
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0.400 | Biomarker | GENOMICS_ENGLAND | |||||||||||
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0.400 | Biomarker | GENOMICS_ENGLAND | |||||||||||
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0.400 | Biomarker | GENOMICS_ENGLAND | |||||||||||
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0.400 | Biomarker | GENOMICS_ENGLAND | |||||||||||
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0.400 | Biomarker | GENOMICS_ENGLAND | |||||||||||
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0.400 | Biomarker | GENOMICS_ENGLAND | |||||||||||
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0.400 | Biomarker | GENOMICS_ENGLAND | |||||||||||
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0.400 | Biomarker | GENOMICS_ENGLAND | |||||||||||
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0.400 | Biomarker | GENOMICS_ENGLAND | |||||||||||
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0.300 | Biomarker | GENOMICS_ENGLAND | |||||||||||
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0.300 | Biomarker | GENOMICS_ENGLAND | |||||||||||
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0.300 | Biomarker | GENOMICS_ENGLAND | |||||||||||
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0.300 | Biomarker | GENOMICS_ENGLAND | |||||||||||
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0.640 | Biomarker | GENOMICS_ENGLAND | Stop codon in the procollagen II gene (COL2A1) in a family with the Stickler syndrome (arthro-ophthalmopathy). | 1677770 | 1991 |
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0.400 | Biomarker | GENOMICS_ENGLAND | Functional and clinical characterization of KCNJ2 mutations associated with LQT7 (Andersen syndrome). | 12163457 | 2002 |
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0.420 | Biomarker | GENOMICS_ENGLAND | Loss of DNA-dependent dimerization of the transcription factor SOX9 as a cause for campomelic dysplasia. | 12783851 | 2003 |
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0.890 | Biomarker | GENOMICS_ENGLAND | The del(2)(q32.2q33) deletion syndrome defined by clinical and molecular characterization of four patients. | 16179223 | 2005 |