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 | 15 | 0.600 | strong | 1.000 | 3 | 15 | 2015 | 2018 | |||||
|
disease | Nervous System Diseases | Disease or Syndrome | 187 | 126 | 0.110 | None | 1.000 | 1 | 2 | 2019 | 2019 | ||||
|
disease | Mental or Behavioral Dysfunction | 1825 | 553 | 0.110 | None | 1.000 | 1 | 2 | 2018 | 2018 | |||||
|
phenotype | Clinical Attribute | 507 | 1037 | 0.100 | None | 1.000 | 1 | 1 | 2019 | 2019 | |||||
|
phenotype | Laboratory or Test Result | 139 | 296 | 0.100 | None | 1.000 | 1 | 2 | 2016 | 2016 | |||||
|
phenotype | Laboratory Procedure | 57 | 76 | 0.100 | None | 1.000 | 1 | 1 | 2019 | 2019 | |||||
|
phenotype | Laboratory Procedure | 139 | 296 | 0.100 | None | 1.000 | 1 | 2 | 2016 | 2016 | |||||
|
disease | Skin and Connective Tissue Diseases; Musculoskeletal Diseases; Immune System Diseases | Disease or Syndrome | 2723 | 2387 | 0.100 | None | 1.000 | 1 | 1 | 2011 | 2011 | ||||
|
disease | Hemic and Lymphatic Diseases | Disease or Syndrome | 413 | 787 | 0.100 | None | 1.000 | 1 | 1 | 2016 | 2016 | ||||
|
phenotype | Finding | 265 | 23 | 0.100 | None | 0 | |||||||||
|
phenotype | Finding | 160 | 246 | 0.100 | None | 0 | 2 | ||||||||
|
phenotype | Anatomical Abnormality | 104 | 131 | 0.100 | None | 0 | 2 | ||||||||
|
disease | Disease or Syndrome | 321 | 67 | 0.100 | None | 0 | |||||||||
|
disease | Pathological Conditions, Signs and Symptoms; Nervous System Diseases; Mental Disorders; Behavior and Behavior Mechanisms | Mental or Behavioral Dysfunction | 112 | 10 | 0.100 | None | 0 | ||||||||
|
phenotype | Finding | 11 | 4 | 0.100 | None | 0 | |||||||||
|
phenotype | Pathological Conditions, Signs and Symptoms; Nervous System Diseases | Finding | 955 | 164 | 0.100 | None | 0 | ||||||||
|
phenotype | Finding | 426 | 39 | 0.100 | None | 0 | |||||||||
|
phenotype | Finding | 67 | 4 | 0.100 | None | 0 | |||||||||
|
phenotype | Finding | 149 | 5 | 0.100 | None | 0 | |||||||||
|
phenotype | Finding | 83 | 17 | 0.100 | None | 0 | |||||||||
|
disease | Disease or Syndrome | 271 | 13 | 0.100 | None | 0 | |||||||||
|
disease | Eye Diseases | Disease or Syndrome | 148 | 45 | 0.100 | None | 0 | ||||||||
|
group | Digestive System Diseases; Otorhinolaryngologic Diseases | Disease or Syndrome | 389 | 50 | 0.100 | None | 0 | ||||||||
|
disease | Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases; Stomatognathic Diseases | Congenital Abnormality | 586 | 53 | 0.100 | None | 0 | ||||||||
|
disease | Eye Diseases | Disease or Syndrome | 490 | 167 | 0.100 | None | 0 |