Gene | Disease | Score gda | Association Type | Original DB | Sentence supporting the association | PMID | PMID Year | ||||||||
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0.100 | Biomarker | LHGDN | Inflammation at birth is associated with subnormal development in very preterm infants. | 18391842 | 2008 |
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0.100 | GeneticVariation | CLINVAR | Homozygosity for MECP2 gene in a girl with classical Rett syndrome. | 17881312 | 2008 |
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0.100 | Biomarker | LHGDN | Inflammation at birth is associated with subnormal development in very preterm infants. | 18391842 | 2008 |
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0.100 | GeneticVariation | CLINVAR | MECP2 and CDKL5 gene mutation analysis in Chinese patients with Rett syndrome. | 17089071 | 2007 |
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0.100 | GeneticVariation | BEFREE | Carriage of polymorphisms in the tumor necrosis factor-alpha and mannose-binding lectin genes are associated with an increased risk of cerebral palsy. | 16522396 | 2006 |
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0.100 | Biomarker | BEFREE | Factor 5, Factor 2, methylene tetrahydrofolate reductase, tumor necrosis factor-alpha, and other SNPs tested were not significantly associated with CP risk. | 15718364 | 2005 |
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0.100 | GeneticVariation | CLINVAR | Prenatal diagnosis in Rett syndrome. | 12065946 | 2003 |
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0.100 | GeneticVariation | CLINVAR | Chronic osteomyelitis in patients with sickle cell disease. | 10944834 | 2000 |
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0.100 | CausalMutation | CLINVAR | |||||||||||
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0.100 | Biomarker | HPO | |||||||||||
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0.100 | Biomarker | HPO | |||||||||||
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0.100 | CausalMutation | CLINVAR | |||||||||||
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0.100 | Biomarker | HPO | |||||||||||
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0.100 | GeneticVariation | CLINVAR | |||||||||||
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0.100 | CausalMutation | CLINVAR | |||||||||||
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0.100 | Biomarker | HPO | |||||||||||
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0.100 | Biomarker | HPO | |||||||||||
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0.100 | Biomarker | HPO | |||||||||||
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0.100 | Biomarker | HPO | |||||||||||
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0.100 | Biomarker | HPO | |||||||||||
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0.100 | GeneticVariation | CLINVAR | |||||||||||
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0.100 | GeneticVariation | CLINVAR | |||||||||||
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0.100 | CausalMutation | CLINVAR | |||||||||||
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0.100 | Biomarker | HPO | |||||||||||
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0.100 | Biomarker | HPO |