RAF1, Raf-1 proto-oncogene, serine/threonine kinase, 5894
N. diseases: 470; N. variants: 52
Source: ALL
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; Digestive System Diseases | Finding | 523 | 30 | 0.100 | None | 0 | ||||||||
|
phenotype | Finding | 37 | 3 | 0.100 | None | 0 | |||||||||
|
phenotype | Finding | 145 | 10 | 0.100 | None | 0 | |||||||||
|
phenotype | Finding | 407 | 35 | 0.100 | None | 0 | 1 | ||||||||
|
disease | Pathological Conditions, Signs and Symptoms; Skin and Connective Tissue Diseases | Disease or Syndrome | 19 | 3 | 0.300 | 0 | |||||||||
|
phenotype | Finding | 59 | 15 | 0.100 | None | 0 | |||||||||
|
disease | Pathological Conditions, Signs and Symptoms; Cardiovascular Diseases | Disease or Syndrome | 1800 | 680 | 0.100 | None | 0 | ||||||||
|
disease | Congenital Abnormality | 181 | 4 | 0.100 | None | 0 | |||||||||
|
phenotype | Finding | 429 | 29 | 0.100 | None | 0 | |||||||||
|
phenotype | Finding | 159 | 25 | 0.100 | None | 0 | |||||||||
|
phenotype | Finding | 58 | 4 | 0.100 | None | 0 | |||||||||
|
disease | Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Cardiovascular Diseases | Anatomical Abnormality | 55 | 14 | 0.100 | None | 0 | ||||||||
|
phenotype | Hemic and Lymphatic Diseases | Pathologic Function | 71 | 14 | 0.100 | None | 0 | ||||||||
|
disease | Eye Diseases; Nervous System Diseases | Disease or Syndrome | 716 | 89 | 0.100 | None | 0 | 1 | |||||||
|
phenotype | Finding | 96 | 19 | 0.100 | None | 0 | 1 | ||||||||
|
disease | Musculoskeletal Diseases | Disease or Syndrome | 850 | 135 | 0.100 | None | 0 | ||||||||
|
phenotype | Finding | 111 | 16 | 0.100 | None | 0 | |||||||||
|
phenotype | Finding | 426 | 39 | 0.100 | None | 0 | 2 | ||||||||
|
disease | Pathological Conditions, Signs and Symptoms | Disease or Syndrome | 607 | 12 | 0.100 | None | 0 | ||||||||
|
group | Musculoskeletal Diseases; Nervous System Diseases | Disease or Syndrome | 634 | 166 | 0.100 | None | 0 | ||||||||
|
disease | Congenital Abnormality | 284 | 39 | 0.100 | None | 0 | |||||||||
|
disease | Nutritional and Metabolic Diseases; Skin and Connective Tissue Diseases | Disease or Syndrome | 226 | 28 | 0.100 | None | 0 | ||||||||
|
phenotype | Anatomical Abnormality | 46 | 11 | 0.100 | None | 0 | |||||||||
|
phenotype | Finding | 97 | 12 | 0.100 | None | 0 | 1 | ||||||||
|
disease | Cardiovascular Diseases | Disease or Syndrome | 106 | 40 | 0.100 | None | 0 |