SIN3A, SIN3 transcription regulator family member A, 25942
N. diseases: 184; N. variants: 10
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 | Disease or Syndrome | 1 | 7 | 0.600 | strong | 1.000 | 2 | 7 | 2015 | 2019 | |||||
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phenotype | Finding | 1 | 1 | 0.100 | None | 1.000 | 1 | 1 | 2019 | 2019 | |||||
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phenotype | Anatomical Abnormality | 1 | 0.100 | None | 0 | ||||||||||
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disease | Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases | Congenital Abnormality | 2 | 0.300 | None | 1.000 | 1 | 2016 | 2016 | ||||||
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disease | Disease or Syndrome | 3 | 0.100 | None | 0 | ||||||||||
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phenotype | Finding | 4 | 0.100 | None | 0 | ||||||||||
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disease | Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases; Mental Disorders; Behavior and Behavior Mechanisms | Congenital Abnormality | 5 | 0.300 | None | 1.000 | 1 | 2016 | 2016 | ||||||
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phenotype | Sign or Symptom | 5 | 0.100 | None | 0 | ||||||||||
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phenotype | Finding | 5 | 2 | 0.100 | None | 0 | |||||||||
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phenotype | Finding | 6 | 1 | 0.100 | None | 0 | |||||||||
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disease | Nervous System Diseases | Disease or Syndrome | 7 | 0.300 | None | 1.000 | 1 | 2016 | 2016 | ||||||
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disease | Nervous System Diseases | Disease or Syndrome | 7 | 0.300 | None | 1.000 | 1 | 2016 | 2016 | ||||||
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disease | Nervous System Diseases | Congenital Abnormality | 7 | 0.300 | None | 1.000 | 1 | 2016 | 2016 | ||||||
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phenotype | Pathological Conditions, Signs and Symptoms; Eye Diseases; Nervous System Diseases | Finding | 7 | 5 | 0.100 | None | 0 | ||||||||
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disease | Congenital Abnormality | 8 | 2 | 0.100 | None | 0 | |||||||||
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disease | Finding | 9 | 3 | 0.300 | moderate | 1.000 | 1 | 2016 | 2016 | ||||||
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phenotype | Finding | 11 | 2 | 0.100 | None | 0 | |||||||||
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phenotype | Finding | 16 | 3 | 0.100 | None | 0 | |||||||||
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phenotype | Finding | 17 | 0.100 | None | 0 | ||||||||||
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disease | Nervous System Diseases | Disease or Syndrome | 18 | 1 | 0.300 | None | 1.000 | 1 | 2016 | 2016 | |||||
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phenotype | Finding | 19 | 6 | 0.100 | None | 0 | |||||||||
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disease | Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Digestive System Diseases | Disease or Syndrome | 20 | 2 | 0.100 | None | 0 | ||||||||
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disease | Congenital Abnormality | 25 | 3 | 0.100 | None | 0 | |||||||||
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phenotype | Finding | 25 | 3 | 0.100 | None | 0 | |||||||||
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disease | Nervous System Diseases | Disease or Syndrome | 26 | 1 | 0.300 | None | 1.000 | 1 | 2016 | 2016 |