PPP2R3C, protein phosphatase 2 regulatory subunit B''gamma, 55012
N. diseases: 49; 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. | ||||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
disease | Musculoskeletal Diseases | Disease or Syndrome | 710 | 609 | 0.100 | None | 1.000 | 1 | 1 | 2016 | 2016 | ||||
|
disease | Skin and Connective Tissue Diseases | Disease or Syndrome | 1308 | 705 | 0.100 | None | 1.000 | 1 | 1 | 2016 | 2016 | ||||
|
phenotype | Laboratory Procedure | 681 | 1322 | 0.100 | None | 1.000 | 1 | 1 | 2019 | 2019 | |||||
|
phenotype | Laboratory Procedure | 338 | 456 | 0.100 | None | 1.000 | 1 | 1 | 2016 | 2016 | |||||
|
disease | Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Skin and Connective Tissue Diseases; Immune System Diseases | Disease or Syndrome | 751 | 232 | 0.100 | None | 1.000 | 1 | 1 | 2015 | 2015 | ||||
|
disease | Digestive System Diseases | Disease or Syndrome | 1458 | 827 | 0.100 | None | 1.000 | 1 | 1 | 2016 | 2016 | ||||
|
disease | Digestive System Diseases | Disease or Syndrome | 1382 | 1147 | 0.100 | None | 1.000 | 1 | 1 | 2016 | 2016 | ||||
|
disease | Digestive System Diseases | Disease or Syndrome | 188 | 276 | 0.100 | None | 1.000 | 1 | 1 | 2016 | 2016 | ||||
|
phenotype | Finding | 83 | 7 | 0.100 | None | 0 | |||||||||
|
phenotype | Finding | 110 | 13 | 0.100 | None | 0 | |||||||||
|
phenotype | Finding | 46 | 7 | 0.100 | None | 0 | |||||||||
|
phenotype | Finding | 2 | 0.100 | None | 0 | ||||||||||
|
phenotype | Congenital Abnormality | 79 | 8 | 0.100 | None | 0 | |||||||||
|
phenotype | Finding | 105 | 10 | 0.100 | None | 0 | |||||||||
|
phenotype | Finding | 99 | 8 | 0.100 | None | 0 | |||||||||
|
phenotype | Finding | 31 | 6 | 0.100 | None | 0 | |||||||||
|
phenotype | Finding | 42 | 0.100 | None | 0 | ||||||||||
|
phenotype | Finding | 7 | 1 | 0.100 | None | 0 | |||||||||
|
phenotype | Finding | 23 | 0.100 | None | 0 | ||||||||||
|
phenotype | Finding | 26 | 0.100 | None | 0 | ||||||||||
|
phenotype | Finding | 1010 | 0.100 | None | 0 | ||||||||||
|
phenotype | Finding | 137 | 0.100 | None | 0 | ||||||||||
|
phenotype | Finding | 141 | 14 | 0.100 | None | 0 | |||||||||
|
phenotype | Finding | 26 | 2 | 0.100 | None | 0 | |||||||||
|
disease | Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Eye Diseases | Disease or Syndrome | 194 | 33 | 0.100 | None | 0 |