SOS2, SOS Ras/Rho guanine nucleotide exchange factor 2, 6655
N. diseases: 92; N. variants: 7
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. | ||||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
disease | Pathological Conditions, Signs and Symptoms; Skin and Connective Tissue Diseases | Disease or Syndrome | 19 | 3 | 0.300 | 0 | |||||||||
|
phenotype | Finding | 288 | 29 | 0.100 | None | 0 | |||||||||
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disease | Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Skin and Connective Tissue Diseases | Congenital Abnormality | 44 | 0.100 | None | 0 | |||||||||
|
phenotype | Finding | 391 | 49 | 0.100 | None | 0 | |||||||||
|
phenotype | Finding | 1127 | 292 | 0.100 | None | 0 | |||||||||
|
phenotype | Finding | 779 | 0.100 | None | 0 | ||||||||||
|
phenotype | Finding | 60 | 4 | 0.100 | None | 0 | |||||||||
|
disease | Endocrine System Diseases | Disease or Syndrome | 178 | 18 | 0.100 | None | 0 | ||||||||
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phenotype | Finding | 305 | 22 | 0.100 | None | 0 | |||||||||
|
phenotype | Finding | 1010 | 0.100 | None | 0 | ||||||||||
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disease | Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases; Nervous System Diseases; Stomatognathic Diseases | Congenital Abnormality | 497 | 70 | 0.100 | None | 0 | ||||||||
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phenotype | Finding | 211 | 17 | 0.100 | None | 0 | |||||||||
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disease | Cardiovascular Diseases | Anatomical Abnormality | 36 | 2 | 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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disease | Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Skin and Connective Tissue Diseases | Congenital Abnormality | 78 | 19 | 0.100 | None | 0 | ||||||||
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disease | Neoplasms | Neoplastic Process | 43 | 1 | 0.100 | None | 0 | ||||||||
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phenotype | Finding | 295 | 14 | 0.100 | None | 0 | |||||||||
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phenotype | Finding | 24 | 7 | 0.100 | None | 0 | |||||||||
|
phenotype | Finding | 145 | 10 | 0.100 | None | 0 | |||||||||
|
phenotype | Finding | 37 | 3 | 0.100 | None | 0 | |||||||||
|
phenotype | Finding | 58 | 4 | 0.100 | None | 0 | |||||||||
|
phenotype | Finding | 111 | 16 | 0.100 | None | 0 | |||||||||
|
phenotype | Finding | 96 | 19 | 0.100 | None | 0 | |||||||||
|
phenotype | Finding | 59 | 15 | 0.100 | None | 0 | |||||||||
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disease | Congenital Abnormality | 284 | 39 | 0.100 | None | 0 |