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. | ||||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
phenotype | Pathological Conditions, Signs and Symptoms; Nervous System Diseases | Finding | 24 | 4 | 0.100 | None | 0 | ||||||||
|
phenotype | Finding | 1 | 0.100 | None | 0 | ||||||||||
|
disease | Anatomical Abnormality | 12 | 1 | 0.100 | None | 0 | |||||||||
|
disease | Anatomical Abnormality | 40 | 3 | 0.100 | None | 0 | |||||||||
|
disease | Anatomical Abnormality | 41 | 0.100 | None | 0 | ||||||||||
|
disease | Anatomical Abnormality | 40 | 5 | 0.100 | None | 0 | |||||||||
|
phenotype | Finding | 60 | 0.100 | None | 0 | ||||||||||
|
phenotype | Finding | 39 | 0.100 | None | 0 | ||||||||||
|
phenotype | Finding | 117 | 0.100 | None | 0 | ||||||||||
|
phenotype | Finding | 87 | 0.100 | None | 0 | ||||||||||
|
phenotype | Respiratory Tract Diseases | Finding | 85 | 3 | 0.100 | None | 0 | ||||||||
|
phenotype | Finding | 123 | 0.100 | None | 0 | ||||||||||
|
phenotype | Finding | 84 | 3 | 0.100 | None | 0 | |||||||||
|
phenotype | Finding | 223 | 19 | 0.100 | None | 0 | |||||||||
|
phenotype | Pathological Conditions, Signs and Symptoms; Nervous System Diseases | Finding | 955 | 164 | 0.100 | None | 0 | ||||||||
|
phenotype | Finding | 319 | 0.100 | None | 0 | ||||||||||
|
phenotype | Finding | 87 | 0.100 | None | 0 | ||||||||||
|
phenotype | Finding | 2 | 1 | 0.100 | None | 0 | |||||||||
|
phenotype | Pathological Conditions, Signs and Symptoms; Nervous System Diseases | Finding | 31 | 7 | 0.100 | None | 0 | ||||||||
|
phenotype | Finding | 1010 | 0.100 | None | 0 | ||||||||||
|
disease | Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases; Stomatognathic Diseases | Anatomical Abnormality | 191 | 11 | 0.100 | None | 0 | ||||||||
|
phenotype | Finding | 477 | 0.100 | None | 0 | ||||||||||
|
disease | Eye Diseases | Disease or Syndrome | 490 | 167 | 0.100 | None | 0 | ||||||||
|
phenotype | Female Urogenital Diseases and Pregnancy Complications | Pathologic Function | 208 | 28 | 0.100 | None | 0 | ||||||||
|
phenotype | Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases | Finding | 590 | 77 | 0.100 | None | 0 |