SMARCC2, SWI/SNF related, matrix associated, actin dependent regulator of chromatin subfamily c member 2, 6601
N. diseases: 78; N. variants: 0
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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group | Pathological Conditions, Signs and Symptoms; Nervous System Diseases; Mental Disorders; Behavior and Behavior Mechanisms | Mental or Behavioral Dysfunction | 2165 | 159 | 0.410 | strong | 1.000 | 1 | 2019 | 2019 | |||||
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disease | Mental or Behavioral Dysfunction | 1825 | 553 | 0.410 | strong | 1.000 | 1 | 2019 | 2019 | ||||||
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disease | Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases; Nervous System Diseases; Mental Disorders; Stomatognathic Diseases; Behavior and Behavior Mechanisms | Disease or Syndrome | 56 | 6 | 0.300 | None | 1.000 | 1 | 2019 | 2019 | |||||
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phenotype | Finding | 73 | 2 | 0.100 | None | 0 | |||||||||
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phenotype | Finding | 85 | 7 | 0.100 | None | 0 | |||||||||
|
phenotype | Pathological Conditions, Signs and Symptoms; Nervous System Diseases | Finding | 955 | 164 | 0.100 | None | 0 | ||||||||
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phenotype | Finding | 104 | 13 | 0.100 | None | 0 | |||||||||
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phenotype | Finding | 429 | 29 | 0.100 | None | 0 | |||||||||
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phenotype | Pathological Conditions, Signs and Symptoms; Skin and Connective Tissue Diseases | Finding | 113 | 3 | 0.100 | None | 0 | ||||||||
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phenotype | Finding | 83 | 17 | 0.100 | None | 0 | |||||||||
|
phenotype | Finding | 779 | 0.100 | None | 0 | ||||||||||
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phenotype | Pathological Conditions, Signs and Symptoms | Finding | 194 | 33 | 0.100 | None | 0 | ||||||||
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phenotype | Finding | 117 | 1 | 0.100 | None | 0 | |||||||||
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phenotype | Finding | 407 | 35 | 0.100 | None | 0 | |||||||||
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phenotype | Finding | 85 | 3 | 0.100 | None | 0 | |||||||||
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phenotype | Finding | 145 | 10 | 0.100 | None | 0 | |||||||||
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phenotype | Finding | 103 | 31 | 0.100 | None | 0 | |||||||||
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phenotype | Finding | 426 | 39 | 0.100 | None | 0 | |||||||||
|
phenotype | Finding | 35 | 1 | 0.100 | None | 0 | |||||||||
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phenotype | Finding | 182 | 25 | 0.100 | None | 0 | |||||||||
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phenotype | Finding | 65 | 1 | 0.100 | None | 0 | |||||||||
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disease | Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Cardiovascular Diseases | Congenital Abnormality | 198 | 13 | 0.100 | None | 0 | ||||||||
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disease | Anatomical Abnormality | 30 | 0.100 | None | 0 | ||||||||||
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disease | Anatomical Abnormality | 11 | 3 | 0.100 | None | 0 | |||||||||
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disease | Anatomical Abnormality | 10 | 0.100 | None | 0 |