CHD7, chromodomain helicase DNA binding protein 7, 55636
N. diseases: 419; N. variants: 247
Source: ALL
Disease | Type | Disease Class | Semantic Type | N. genes d | N. SNPs d | Score gda | EL gda | EI gda | N. PMIDs | N. SNPs gda | First Ref. | Last Ref. | ||||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
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disease | Congenital Abnormality | 439 | 617 | 0.110 | None | 1.000 | 21 | 7 | 1999 | 2016 | |||||
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disease | Disease or Syndrome | 1 | 25 | 0.600 | strong | 1.000 | 10 | 25 | 2004 | 2016 | |||||
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group | Congenital Abnormality | 126 | 6 | 0.040 | None | 0.750 | 4 | 2009 | 2012 | ||||||
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disease | Congenital Abnormality | 161 | 44 | 0.030 | None | 1.000 | 3 | 2008 | 2011 | ||||||
|
phenotype | Laboratory Procedure | 681 | 1322 | 0.100 | None | 1.000 | 3 | 3 | 2016 | 2019 | |||||
|
phenotype | Laboratory Procedure | 610 | 1144 | 0.100 | None | 1.000 | 3 | 6 | 2016 | 2019 | |||||
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phenotype | Laboratory Procedure | 145 | 234 | 0.100 | None | 1.000 | 2 | 2 | 2016 | 2018 | |||||
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disease | Congenital Abnormality | 44 | 1 | 0.020 | None | 1.000 | 2 | 2006 | 2014 | ||||||
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phenotype | Disease or Syndrome | 84 | 7 | 0.020 | None | 1.000 | 2 | 1991 | 2018 | ||||||
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disease | Congenital Abnormality | 51 | 45 | 0.020 | None | 1.000 | 2 | 2013 | 2014 | ||||||
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phenotype | Organism Attribute | 1903 | 3972 | 0.100 | None | 1.000 | 1 | 1 | 2019 | 2019 | |||||
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phenotype | Clinical Attribute | 430 | 746 | 0.100 | None | 1.000 | 1 | 1 | 2019 | 2019 | |||||
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phenotype | Laboratory Procedure | 272 | 452 | 0.100 | None | 1.000 | 1 | 3 | 2016 | 2016 | |||||
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disease | Congenital Abnormality | 1 | 0.010 | None | 1.000 | 1 | 1991 | 1991 | |||||||
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disease | Acquired Abnormality | 155 | 2 | 0.010 | None | 1.000 | 1 | 1 | 2008 | 2008 | |||||
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disease | Disease or Syndrome | 16 | 7 | 0.010 | None | 1.000 | 1 | 2019 | 2019 | ||||||
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disease | Congenital Abnormality | 8 | 1 | 0.010 | None | 1.000 | 1 | 1991 | 1991 | ||||||
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group | Congenital Abnormality | 67 | 2 | 0.010 | None | 1.000 | 1 | 2007 | 2007 | ||||||
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disease | Disease or Syndrome | 55 | 28 | 0.010 | None | 1.000 | 1 | 2019 | 2019 | ||||||
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phenotype | Disease or Syndrome | 716 | 25 | 0.010 | None | 1.000 | 1 | 2017 | 2017 | ||||||
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phenotype | Laboratory Procedure | 100 | 150 | 0.100 | None | 1.000 | 1 | 1 | 2016 | 2016 | |||||
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group | Disease or Syndrome | 29 | 2 | 0.010 | None | < 0.001 | 1 | 2018 | 2018 | ||||||
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phenotype | Neoplastic Process | 6626 | 169 | 0.010 | None | 1.000 | 1 | 2019 | 2019 | ||||||
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phenotype | Finding | 129 | 209 | 0.100 | None | 1.000 | 1 | 1 | 2015 | 2015 | |||||
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disease | Finding | 578 | 1158 | 0.400 | strong | 1.000 | 1 | 1 | 2018 | 2018 |