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 | Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Skin and Connective Tissue Diseases | Disease or Syndrome | 1 | 1 | 0.620 | None | 1.000 | 3 | 1 | 2010 | 2017 | ||||
|
disease | Disease or Syndrome | 1 | 3 | 0.400 | strong | 1.000 | 1 | 3 | 2018 | 2018 | |||||
|
disease | Eye Diseases | Disease or Syndrome | 94 | 74 | 0.310 | None | 1.000 | 2 | 2017 | 2018 | |||||
|
group | Immune System Diseases | Disease or Syndrome | 973 | 31 | 0.110 | None | 1.000 | 1 | 1 | 2016 | 2016 | ||||
|
disease | Musculoskeletal Diseases | Anatomical Abnormality | 656 | 1178 | 0.100 | None | 1.000 | 1 | 1 | 2018 | 2018 | ||||
|
phenotype | Laboratory Procedure | 131 | 224 | 0.100 | None | 1.000 | 1 | 1 | 2016 | 2016 | |||||
|
disease | Finding | 578 | 1158 | 0.100 | None | 1.000 | 1 | 1 | 2018 | 2018 | |||||
|
phenotype | Finding | 2 | 2 | 0.100 | None | 0 | 1 | ||||||||
|
phenotype | Hemic and Lymphatic Diseases | Finding | 4 | 1 | 0.100 | None | 0 | 1 | |||||||
|
phenotype | Immune System Diseases; Hemic and Lymphatic Diseases | Finding | 5 | 1 | 0.100 | None | 0 | 1 | |||||||
|
phenotype | Finding | 12 | 8 | 0.100 | None | 0 | 1 | ||||||||
|
disease | Congenital, Hereditary, and Neonatal Diseases and Abnormalities | Congenital Abnormality | 6 | 0.100 | None | 0 | |||||||||
|
phenotype | Pathologic Function | 32 | 37 | 0.100 | None | 0 | 1 | ||||||||
|
phenotype | Hemic and Lymphatic Diseases | Disease or Syndrome | 277 | 5 | 0.100 | None | 0 | ||||||||
|
phenotype | Finding | 9 | 0.100 | None | 0 | ||||||||||
|
disease | Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases | Congenital Abnormality | 160 | 7 | 0.100 | None | 0 | ||||||||
|
phenotype | Finding | 212 | 9 | 0.100 | None | 0 | 1 | ||||||||
|
phenotype | Finding | 1 | 1 | 0.100 | None | 0 | 1 | ||||||||
|
phenotype | Anatomical Abnormality | 1 | 1 | 0.100 | None | 0 | 1 | ||||||||
|
phenotype | Finding | 22 | 0.100 | None | 0 | ||||||||||
|
disease | Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Skin and Connective Tissue Diseases | Disease or Syndrome | 165 | 19 | 0.100 | None | 0 | ||||||||
|
disease | Congenital Abnormality | 148 | 18 | 0.100 | None | 0 | |||||||||
|
phenotype | Finding | 1 | 1 | 0.100 | None | 0 | 1 | ||||||||
|
phenotype | Finding | 1 | 1 | 0.100 | None | 0 | 1 | ||||||||
|
disease | Anatomical Abnormality | 26 | 1 | 0.100 | None | 0 | 1 |