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 | Disease or Syndrome | 1 | 1 | 0.500 | None | 1.000 | 1 | 1 | 2017 | 2017 | |||||
|
disease | Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Skin and Connective Tissue Diseases | Disease or Syndrome | 4 | 0.300 | None | 1.000 | 1 | 2017 | 2017 | ||||||
|
disease | Digestive System Diseases; Neoplasms | Neoplastic Process | 5473 | 1962 | 0.300 | None | 0 | 1 | |||||||
|
phenotype | Laboratory Procedure | 545 | 1440 | 0.100 | None | 1.000 | 3 | 2 | 2016 | 2018 | |||||
|
phenotype | Laboratory Procedure | 483 | 1142 | 0.100 | None | 1.000 | 2 | 1 | 2015 | 2018 | |||||
|
phenotype | Laboratory Procedure | 135 | 624 | 0.100 | None | 1.000 | 1 | 1 | 2016 | 2016 | |||||
|
phenotype | Laboratory Procedure | 563 | 1418 | 0.100 | None | 1.000 | 1 | 1 | 2018 | 2018 | |||||
|
phenotype | Laboratory Procedure | 264 | 1463 | 0.100 | None | 1.000 | 1 | 1 | 2019 | 2019 | |||||
|
phenotype | Clinical Attribute | 843 | 1931 | 0.100 | None | 1.000 | 1 | 1 | 2018 | 2018 | |||||
|
phenotype | Finding | 77 | 4 | 0.100 | None | 0 | |||||||||
|
disease | Pathological Conditions, Signs and Symptoms; Skin and Connective Tissue Diseases | Disease or Syndrome | 176 | 19 | 0.100 | None | 0 | ||||||||
|
phenotype | Finding | 58 | 5 | 0.100 | None | 0 | |||||||||
|
phenotype | Finding | 1 | 0.100 | None | 0 | ||||||||||
|
phenotype | Finding | 95 | 15 | 0.100 | None | 0 | |||||||||
|
phenotype | Finding | 159 | 25 | 0.100 | None | 0 | |||||||||
|
phenotype | Finding | 117 | 1 | 0.100 | None | 0 | |||||||||
|
phenotype | Skin and Connective Tissue Diseases | Finding | 10 | 0.100 | None | 0 | |||||||||
|
phenotype | Finding | 57 | 0.100 | None | 0 | ||||||||||
|
phenotype | Finding | 87 | 0.100 | None | 0 | ||||||||||
|
phenotype | Stomatognathic Diseases | Finding | 20 | 0.100 | None | 0 | |||||||||
|
phenotype | Respiratory Tract Diseases; Otorhinolaryngologic Diseases | Finding | 10 | 1 | 0.100 | None | 0 | ||||||||
|
disease | Skin and Connective Tissue Diseases | Disease or Syndrome | 863 | 368 | 0.100 | None | 0 | ||||||||
|
disease | Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Stomatognathic Diseases | Congenital Abnormality | 218 | 48 | 0.100 | None | 0 | ||||||||
|
disease | Skin and Connective Tissue Diseases | Disease or Syndrome | 69 | 1 | 0.100 | None | 0 | ||||||||
|
disease | Skin and Connective Tissue Diseases | Disease or Syndrome | 69 | 2 | 0.100 | None | 0 |