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 Abnormality | 113 | 5 | 0.100 | None | 0 | |||||||||
|
disease | Respiratory Tract Diseases | Disease or Syndrome | 14 | 0.100 | None | 0 | |||||||||
|
phenotype | Finding | 33 | 4 | 0.100 | None | 0 | |||||||||
|
disease | Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Stomatognathic Diseases | Disease or Syndrome | 40 | 10 | 0.100 | None | 0 | ||||||||
|
disease | Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases; Mental Disorders | Congenital Abnormality | 226 | 26 | 0.100 | None | 0 | ||||||||
|
phenotype | Nutritional and Metabolic Diseases; Nervous System Diseases | Finding | 103 | 8 | 0.100 | None | 0 | ||||||||
|
phenotype | Finding | 1127 | 292 | 0.100 | None | 0 | |||||||||
|
phenotype | Finding | 74 | 1 | 0.100 | None | 0 | |||||||||
|
phenotype | Immune System Diseases | Finding | 30 | 0.100 | None | 0 | |||||||||
|
phenotype | Finding | 64 | 5 | 0.100 | None | 0 | |||||||||
|
phenotype | Finding | 23 | 1 | 0.100 | None | 0 | |||||||||
|
disease | Anatomical Abnormality | 19 | 0.100 | None | 0 | ||||||||||
|
phenotype | Cardiovascular Diseases | Finding | 56 | 3 | 0.100 | None | 0 | ||||||||
|
disease | Disease or Syndrome | 6 | 0.100 | None | 0 | ||||||||||
|
phenotype | Finding | 29 | 0.100 | None | 0 | ||||||||||
|
phenotype | Skin and Connective Tissue Diseases | Finding | 42 | 0.100 | None | 0 | |||||||||
|
phenotype | Anatomical Abnormality | 25 | 0.100 | None | 0 | ||||||||||
|
disease | Anatomical Abnormality | 23 | 0.100 | None | 0 | ||||||||||
|
disease | Anatomical Abnormality | 31 | 0.100 | None | 0 | ||||||||||
|
phenotype | Finding | 14 | 0.100 | None | 0 | ||||||||||
|
phenotype | Finding | 14 | 0.100 | None | 0 | ||||||||||
|
disease | Disease or Syndrome | 271 | 13 | 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 | ||||||||
|
group | Anatomical Abnormality | 29 | 1 | 0.100 | None | 0 | |||||||||
|
phenotype | Pathological Conditions, Signs and Symptoms | Pathologic Function | 41 | 0.100 | None | 0 |