SMARCD2, SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily d, member 2, 6603
N. diseases: 31; N. variants: 4
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 | Neoplasms | Neoplastic Process | 3111 | 6892 | 0.020 | None | 1.000 | 2 | 2017 | 2018 | |||||
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disease | Hemic and Lymphatic Diseases | Disease or Syndrome | 2 | 0.300 | None | 1.000 | 1 | 2017 | 2017 | ||||||
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disease | Neoplasms | Neoplastic Process | 1740 | 140 | 0.010 | None | 1.000 | 1 | 2017 | 2017 | |||||
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disease | Hemic and Lymphatic Diseases | Disease or Syndrome | 389 | 97 | 0.400 | None | 1.000 | 1 | 2017 | 2017 | |||||
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group | Neoplasms | Neoplastic Process | 10161 | 1644 | 0.010 | None | 1.000 | 1 | 2017 | 2017 | |||||
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disease | Neoplasms | Neoplastic Process | 385 | 7 | 0.300 | None | 1.000 | 1 | 2017 | 2017 | |||||
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disease | Neoplasms | Neoplastic Process | 18 | 0.300 | None | 1.000 | 1 | 2017 | 2017 | ||||||
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disease | Neoplasms | Neoplastic Process | 2111 | 144 | 0.010 | None | 1.000 | 1 | 2017 | 2017 | |||||
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disease | Otorhinolaryngologic Diseases | Disease or Syndrome | 120 | 11 | 0.100 | None | 0 | ||||||||
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phenotype | Finding | 85 | 9 | 0.100 | None | 0 | |||||||||
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phenotype | Finding | 1 | 0.100 | None | 0 | ||||||||||
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phenotype | Finding | 62 | 6 | 0.100 | None | 0 | |||||||||
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phenotype | Infections | Finding | 69 | 0.100 | None | 0 | |||||||||
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group | Hemic and Lymphatic Diseases | Neoplastic Process | 1033 | 95 | 0.100 | None | 0 | ||||||||
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phenotype | Finding | 68 | 0.100 | None | 0 | ||||||||||
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disease | Infections; Respiratory Tract Diseases | Finding | 62 | 11 | 0.100 | None | 0 | ||||||||
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phenotype | Pathological Conditions, Signs and Symptoms | Sign or Symptom | 632 | 63 | 0.100 | None | 0 | ||||||||
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disease | Congenital Abnormality | 489 | 64 | 0.100 | None | 0 | |||||||||
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disease | Pathological Conditions, Signs and Symptoms | Disease or Syndrome | 842 | 10 | 0.100 | None | 0 | ||||||||
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disease | Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases | Congenital Abnormality | 325 | 43 | 0.100 | None | 0 | ||||||||
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phenotype | Pathological Conditions, Signs and Symptoms; Skin and Connective Tissue Diseases | Finding | 88 | 17 | 0.100 | None | 0 | ||||||||
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disease | Congenital Abnormality | 181 | 4 | 0.100 | None | 0 | |||||||||
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disease | Nutritional and Metabolic Diseases; Musculoskeletal Diseases | Disease or Syndrome | 845 | 61 | 0.100 | None | 0 | ||||||||
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phenotype | Clinical Attribute | 430 | 746 | 0.100 | None | 1.000 | 1 | 1 | 2019 | 2019 | |||||
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disease | Otorhinolaryngologic Diseases | Disease or Syndrome | 12 | 2 | 0.100 | None | 0 | 2 |