PPARG, peroxisome proliferator activated receptor gamma, 5468
N. diseases: 877; N. variants: 101
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 | Disease or Syndrome | 71 | 4 | 0.100 | None | 0 | ||||||||
|
phenotype | Anatomical Abnormality | 31 | 24 | 0.100 | None | 0 | |||||||||
|
disease | Anatomical Abnormality | 12 | 0.100 | None | 0 | ||||||||||
|
disease | Pathological Conditions, Signs and Symptoms; Cardiovascular Diseases | Disease or Syndrome | 60 | 9 | 0.100 | None | 0 | ||||||||
|
phenotype | Pathologic Function | 25 | 1 | 0.100 | None | 0 | |||||||||
|
phenotype | Finding | 77 | 4 | 0.100 | None | 0 | |||||||||
|
phenotype | Pathological Conditions, Signs and Symptoms | Finding | 49 | 0.100 | None | 0 | |||||||||
|
phenotype | Finding | 35 | 7 | 0.100 | None | 0 | |||||||||
|
phenotype | Finding | 1 | 1 | 0.100 | None | 0 | 1 | ||||||||
|
phenotype | Anatomical Abnormality | 24 | 0.100 | None | 0 | ||||||||||
|
phenotype | Finding | 12 | 0.100 | None | 0 | ||||||||||
|
disease | Pathological Conditions, Signs and Symptoms | Disease or Syndrome | 842 | 10 | 0.100 | None | 0 | ||||||||
|
phenotype | Finding | 1 | 0.100 | None | 0 | ||||||||||
|
phenotype | Anatomical Abnormality | 8 | 0.100 | None | 0 | ||||||||||
|
phenotype | Finding | 4 | 0.100 | None | 0 | ||||||||||
|
phenotype | Finding | 4 | 0.100 | None | 0 | ||||||||||
|
phenotype | Nervous System Diseases | Finding | 410 | 0.100 | None | 0 | |||||||||
|
phenotype | Pathological Conditions, Signs and Symptoms; Cardiovascular Diseases | Finding | 63 | 2 | 0.100 | None | 0 | ||||||||
|
disease | Nutritional and Metabolic Diseases | Disease or Syndrome | 20 | 10 | 0.100 | None | 0 | ||||||||
|
phenotype | Finding | 25 | 0.100 | None | 0 | ||||||||||
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disease | Digestive System Diseases | Disease or Syndrome | 293 | 20 | 0.100 | None | 0 | ||||||||
|
phenotype | Finding | 58 | 5 | 0.100 | None | 0 | |||||||||
|
group | Musculoskeletal Diseases; Nervous System Diseases | Disease or Syndrome | 634 | 166 | 0.100 | None | 0 | ||||||||
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phenotype | Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases | Finding | 12 | 2 | 0.100 | None | 0 | ||||||||
|
group | Nervous System Diseases | Disease or Syndrome | 549 | 69 | 0.100 | None | 0 |