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 | Nutritional and Metabolic Diseases | Disease or Syndrome | 69 | 5 | 0.100 | None | 0 | ||||||||
|
phenotype | Musculoskeletal Diseases | Finding | 60 | 6 | 0.100 | None | 0 | ||||||||
|
phenotype | Finding | 67 | 6 | 0.100 | None | 0 | |||||||||
|
phenotype | Finding | 42 | 5 | 0.100 | None | 0 | |||||||||
|
phenotype | Finding | 5 | 0.100 | None | 0 | ||||||||||
|
phenotype | Finding | 14 | 0.100 | None | 0 | ||||||||||
|
phenotype | Finding | 5 | 0.100 | None | 0 | ||||||||||
|
phenotype | Finding | 7 | 0.100 | None | 0 | ||||||||||
|
phenotype | Musculoskeletal Diseases | Finding | 25 | 0.100 | None | 0 | |||||||||
|
phenotype | Finding | 45 | 6 | 0.100 | None | 0 | |||||||||
|
phenotype | Anatomical Abnormality | 4 | 0.100 | None | 0 | ||||||||||
|
disease | Pathological Conditions, Signs and Symptoms; Nervous System Diseases; Mental Disorders; Behavior and Behavior Mechanisms | Disease or Syndrome | 393 | 2 | 0.100 | None | 0 | ||||||||
|
phenotype | Pathologic Function | 244 | 40 | 0.100 | None | 0 | |||||||||
|
phenotype | Pathological Conditions, Signs and Symptoms; Musculoskeletal Diseases; Nervous System Diseases | Sign or Symptom | 536 | 87 | 0.100 | None | 0 | ||||||||
|
phenotype | Pathological Conditions, Signs and Symptoms; Musculoskeletal Diseases | Sign or Symptom | 139 | 0.100 | None | 0 | |||||||||
|
phenotype | Nutritional and Metabolic Diseases; Musculoskeletal Diseases | Finding | 55 | 0.100 | None | 0 | |||||||||
|
disease | Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases | Congenital Abnormality | 321 | 22 | 0.100 | None | 0 | ||||||||
|
phenotype | Finding | 139 | 4 | 0.100 | None | 0 | |||||||||
|
phenotype | Pathological Conditions, Signs and Symptoms; Nervous System Diseases | Sign or Symptom | 21 | 14 | 0.100 | None | 0 | ||||||||
|
phenotype | Finding | 18 | 1 | 0.100 | None | 0 | |||||||||
|
phenotype | Pathological Conditions, Signs and Symptoms | Finding | 224 | 30 | 0.100 | None | 0 | ||||||||
|
phenotype | Finding | 1127 | 292 | 0.100 | None | 0 | |||||||||
|
phenotype | Finding | 10 | 1 | 0.100 | None | 0 | |||||||||
|
phenotype | Finding | 34 | 0.100 | None | 0 | ||||||||||
|
phenotype | Finding | 8 | 0.100 | None | 0 |