CYP2R1, cytochrome P450 family 2 subfamily R member 1, 120227
N. diseases: 139; N. variants: 11
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 | Finding | 3 | 0.100 | None | 0 | ||||||||||
|
phenotype | Behavior and Behavior Mechanisms | Mental Process | 147 | 14 | 0.100 | None | 0 | ||||||||
|
phenotype | Finding | 1010 | 0.100 | None | 0 | ||||||||||
|
phenotype | Finding | 123 | 0.100 | None | 0 | ||||||||||
|
disease | Nutritional and Metabolic Diseases; Musculoskeletal Diseases | Disease or Syndrome | 47 | 0.100 | None | 0 | |||||||||
|
phenotype | Finding | 5 | 0.100 | None | 0 | ||||||||||
|
disease | Musculoskeletal Diseases | Anatomical Abnormality | 9 | 2 | 0.100 | None | 0 | ||||||||
|
phenotype | Anatomical Abnormality | 3 | 0.100 | None | 0 | ||||||||||
|
disease | Nutritional and Metabolic Diseases; Musculoskeletal Diseases | Disease or Syndrome | 7 | 0.100 | None | 0 | |||||||||
|
phenotype | Finding | 140 | 0.100 | None | 0 | ||||||||||
|
phenotype | Finding | 13 | 0.100 | None | 0 | ||||||||||
|
phenotype | Finding | 121 | 11 | 0.100 | None | 0 | |||||||||
|
phenotype | Finding | 6 | 0.100 | None | 0 | ||||||||||
|
phenotype | Finding | 11 | 0.100 | None | 0 | ||||||||||
|
phenotype | Finding | 4 | 0.100 | None | 0 | ||||||||||
|
phenotype | Finding | 17 | 0.100 | None | 0 | ||||||||||
|
phenotype | Mental Disorders | Finding | 384 | 34 | 0.100 | None | 0 | ||||||||
|
phenotype | Finding | 25 | 2 | 0.100 | None | 0 | |||||||||
|
disease | Nutritional and Metabolic Diseases | Disease or Syndrome | 11 | 0.100 | None | 0 | |||||||||
|
phenotype | Finding | 8 | 0.100 | None | 0 | ||||||||||
|
phenotype | Pathological Conditions, Signs and Symptoms; Nervous System Diseases | Finding | 955 | 164 | 0.100 | None | 0 | ||||||||
|
phenotype | Musculoskeletal Diseases | Finding | 38 | 13 | 0.100 | None | 0 | ||||||||
|
phenotype | Finding | 67 | 0.100 | None | 0 | ||||||||||
|
phenotype | Finding | 67 | 0.100 | None | 0 | ||||||||||
|
disease | Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Stomatognathic Diseases | Disease or Syndrome | 72 | 1 | 0.100 | None | 0 |