IRAK1, interleukin 1 receptor associated kinase 1, 3654
N. diseases: 200; N. variants: 5
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. | ||||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
phenotype | Neoplastic Process | 6626 | 169 | 0.040 | None | 1.000 | 4 | 2011 | 2019 | ||||||
|
disease | Disease or Syndrome | 593 | 24 | 0.010 | None | 1.000 | 1 | 2018 | 2018 | ||||||
|
disease | Disease or Syndrome | 88 | 1 | 0.010 | None | 1.000 | 1 | 2018 | 2018 | ||||||
|
phenotype | Finding | 36 | 0.100 | None | 0 | ||||||||||
|
phenotype | Finding | 35 | 0.100 | None | 0 | ||||||||||
|
phenotype | Finding | 6 | 0.100 | None | 0 | ||||||||||
|
phenotype | Laboratory Procedure | 5 | 0.100 | None | 0 | ||||||||||
|
phenotype | Finding | 12 | 0.100 | None | 0 | ||||||||||
|
phenotype | Laboratory or Test Result | 15 | 0.100 | None | 0 | ||||||||||
|
phenotype | Finding | 18 | 0.100 | None | 0 | ||||||||||
|
phenotype | Finding | 5 | 0.100 | None | 0 | ||||||||||
|
phenotype | Finding | 5 | 0.100 | None | 0 | ||||||||||
|
phenotype | Finding | 27 | 0.100 | None | 0 | ||||||||||
|
disease | Cardiovascular Diseases | Disease or Syndrome | 2006 | 267 | 0.040 | None | 1.000 | 4 | 2005 | 2016 | |||||
|
disease | Cardiovascular Diseases | Disease or Syndrome | 2044 | 281 | 0.040 | None | 1.000 | 4 | 2005 | 2016 | |||||
|
disease | Cardiovascular Diseases | Disease or Syndrome | 1708 | 1577 | 0.330 | None | 0.667 | 3 | 1 | 2010 | 2017 | ||||
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disease | Cardiovascular Diseases | Disease or Syndrome | 1282 | 440 | 0.300 | None | 1.000 | 1 | 2010 | 2010 | |||||
|
group | Cardiovascular Diseases | Disease or Syndrome | 2322 | 1085 | 0.010 | None | 1.000 | 1 | 2008 | 2008 | |||||
|
disease | Cardiovascular Diseases | Disease or Syndrome | 98 | 10 | 0.100 | None | 0 | ||||||||
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disease | Cardiovascular Diseases | Disease or Syndrome | 63 | 1 | 0.100 | None | 0 | ||||||||
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disease | Congenital, Hereditary, and Neonatal Diseases and Abnormalities | Congenital Abnormality | 138 | 6 | 0.010 | None | 1.000 | 1 | 2016 | 2016 | |||||
|
phenotype | Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Digestive System Diseases | Anatomical Abnormality | 14 | 1 | 0.100 | None | 0 | ||||||||
|
disease | Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Eye Diseases; Skin and Connective Tissue Diseases; Stomatognathic Diseases; Cardiovascular Diseases | Disease or Syndrome | 502 | 243 | 0.010 | None | < 0.001 | 1 | 2018 | 2018 | |||||
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disease | Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Hemic and Lymphatic Diseases | Disease or Syndrome | 30 | 18 | 0.010 | None | 1.000 | 1 | 2016 | 2016 | |||||
|
disease | Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases | Mental or Behavioral Dysfunction | 11 | 8 | 0.310 | limited | 1.000 | 2 | 2017 | 2018 |