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 | Finding | 105 | 3 | 0.100 | None | 0 | |||||||||
|
disease | Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases | Congenital Abnormality | 321 | 22 | 0.100 | None | 0 | 1 | |||||||
|
disease | Anatomical Abnormality | 3 | 0.100 | None | 0 | ||||||||||
|
phenotype | Finding | 172 | 1 | 0.100 | None | 0 | |||||||||
|
phenotype | Skin and Connective Tissue Diseases | Sign or Symptom | 159 | 12 | 0.100 | None | 0 | 1 | |||||||
|
disease | Congenital, Hereditary, and Neonatal Diseases and Abnormalities | Congenital Abnormality | 7 | 0.100 | None | 0 | |||||||||
|
phenotype | Finding | 1 | 0.100 | None | 0 | ||||||||||
|
phenotype | Finding | 139 | 4 | 0.100 | None | 0 | |||||||||
|
phenotype | Finding | 41 | 10 | 0.100 | None | 0 | |||||||||
|
phenotype | Skin and Connective Tissue Diseases; Nervous System Diseases | Finding | 5 | 7 | 0.100 | None | 0 | 1 | |||||||
|
disease | Congenital Abnormality | 33 | 1 | 0.100 | None | 0 | |||||||||
|
phenotype | Finding | 7 | 0.100 | None | 0 | ||||||||||
|
phenotype | Finding | 77 | 4 | 0.100 | None | 0 | 1 | ||||||||
|
phenotype | Congenital Abnormality | 79 | 8 | 0.100 | None | 0 | |||||||||
|
phenotype | Finding | 426 | 39 | 0.100 | None | 0 | 1 | ||||||||
|
phenotype | Finding | 95 | 15 | 0.100 | None | 0 | |||||||||
|
phenotype | Finding | 85 | 3 | 0.100 | None | 0 | |||||||||
|
disease | Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Stomatognathic Diseases | Congenital Abnormality | 17 | 2 | 0.100 | None | 0 | 1 | |||||||
|
disease | Disease or Syndrome | 45 | 1 | 0.100 | None | 0 | 1 | ||||||||
|
phenotype | Finding | 117 | 1 | 0.100 | None | 0 | |||||||||
|
phenotype | Congenital Abnormality | 21 | 1 | 0.100 | None | 0 | |||||||||
|
phenotype | Finding | 60 | 4 | 0.100 | None | 0 | 1 | ||||||||
|
phenotype | Pathological Conditions, Signs and Symptoms; Respiratory Tract Diseases | Sign or Symptom | 259 | 16 | 0.100 | None | 0 | ||||||||
|
disease | Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Stomatognathic Diseases | Congenital Abnormality | 109 | 6 | 0.100 | None | 0 | ||||||||
|
disease | Congenital Abnormality | 113 | 5 | 0.100 | None | 0 |