BRIP1, BRCA1 interacting protein C-terminal helicase 1, 83990
N. diseases: 194; N. variants: 242
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 | Anatomical Abnormality | 29 | 1 | 0.100 | None | 0 | |||||||||
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disease | Anatomical Abnormality | 32 | 0.100 | None | 0 | ||||||||||
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disease | Anatomical Abnormality | 40 | 0.100 | None | 0 | ||||||||||
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disease | Anatomical Abnormality | 50 | 2 | 0.100 | None | 0 | |||||||||
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phenotype | Cell or Molecular Dysfunction | 34 | 1 | 0.100 | None | 0 | |||||||||
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disease | Anatomical Abnormality | 33 | 1 | 0.100 | None | 0 | |||||||||
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phenotype | Finding | 34 | 0.300 | strong | 1.000 | 1 | 2005 | 2005 | |||||||
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phenotype | Anatomical Abnormality | 22 | 0.100 | None | 0 | ||||||||||
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disease | Anatomical Abnormality | 70 | 0.100 | None | 0 | ||||||||||
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phenotype | Finding | 75 | 8 | 0.100 | None | 0 | |||||||||
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disease | Anatomical Abnormality | 95 | 8 | 0.100 | None | 0 | |||||||||
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disease | Anatomical Abnormality | 22 | 0.100 | None | 0 | ||||||||||
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phenotype | Finding | 24 | 0.100 | None | 0 | ||||||||||
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disease | Neoplasms | Neoplastic Process | 633 | 22 | 0.300 | strong | 1.000 | 1 | 2017 | 2017 | |||||
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disease | Neoplastic Process | 6 | 1 | 0.010 | None | 1.000 | 1 | 1 | 2018 | 2018 | |||||
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disease | Neoplasms; Nervous System Diseases | Neoplastic Process | 405 | 30 | 0.010 | None | 1.000 | 1 | 1 | 2018 | 2018 | ||||
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phenotype | Finding | 40 | 1 | 0.100 | None | 0 | |||||||||
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disease | Hemic and Lymphatic Diseases | Disease or Syndrome | 847 | 94 | 0.010 | None | 1.000 | 1 | 2008 | 2008 | |||||
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disease | Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Digestive System Diseases | Congenital Abnormality | 139 | 9 | 0.100 | None | 0 | ||||||||
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phenotype | Anatomical Abnormality | 22 | 0.100 | None | 0 | ||||||||||
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disease | Anatomical Abnormality | 52 | 0.100 | None | 0 | ||||||||||
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phenotype | Finding | 45 | 0.100 | None | 0 | ||||||||||
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phenotype | Anatomical Abnormality | 22 | 0.100 | None | 0 | ||||||||||
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disease | Eye Diseases | Disease or Syndrome | 148 | 45 | 0.100 | None | 0 | ||||||||
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group | Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Cardiovascular Diseases | Congenital Abnormality | 384 | 96 | 0.100 | None | 0 |