ROR2, receptor tyrosine kinase like orphan receptor 2, 4920
N. diseases: 250; N. variants: 20
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 | 73 | 10 | 0.100 | None | 0 | |||||||||
|
phenotype | Finding | 23 | 0.100 | None | 0 | ||||||||||
|
phenotype | Finding | 7 | 0.100 | None | 0 | ||||||||||
|
phenotype | Finding | 42 | 0.100 | None | 0 | ||||||||||
|
phenotype | Finding | 17 | 0.100 | None | 0 | ||||||||||
|
disease | Male Urogenital Diseases | Congenital Abnormality | 217 | 11 | 0.100 | None | 0 | ||||||||
|
phenotype | Pathological Conditions, Signs and Symptoms; Nervous System Diseases; Otorhinolaryngologic Diseases | Disease or Syndrome | 740 | 337 | 0.100 | None | 0 | ||||||||
|
disease | Digestive System Diseases; Neoplasms | Neoplastic Process | 543 | 432 | 0.300 | None | 0 | 1 | |||||||
|
disease | Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities | Congenital Abnormality | 235 | 0.100 | None | 0 | |||||||||
|
phenotype | Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases; Endocrine System Diseases | Finding | 86 | 6 | 0.300 | None | 0 | ||||||||
|
phenotype | Finding | 426 | 39 | 0.100 | None | 0 | |||||||||
|
phenotype | Finding | 66 | 7 | 0.100 | None | 0 | |||||||||
|
phenotype | Finding | 129 | 21 | 0.100 | None | 0 | |||||||||
|
phenotype | Finding | 20 | 2 | 0.100 | None | 0 | |||||||||
|
phenotype | Pathological Conditions, Signs and Symptoms | Congenital Abnormality | 19 | 0.100 | None | 0 | |||||||||
|
phenotype | Finding | 30 | 0.100 | None | 0 | ||||||||||
|
phenotype | Finding | 110 | 13 | 0.100 | None | 0 | |||||||||
|
phenotype | Finding | 407 | 35 | 0.100 | None | 0 | |||||||||
|
phenotype | Finding | 62 | 6 | 0.100 | None | 0 | |||||||||
|
phenotype | Finding | 85 | 3 | 0.100 | None | 0 | |||||||||
|
phenotype | Finding | 79 | 8 | 0.100 | None | 0 | |||||||||
|
disease | Musculoskeletal Diseases | Disease or Syndrome | 20 | 17 | 0.100 | None | 0 | ||||||||
|
disease | Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases | Congenital Abnormality | 123 | 10 | 0.100 | None | 0 | ||||||||
|
disease | Congenital Abnormality | 417 | 30 | 0.100 | None | 0 | |||||||||
|
phenotype | Congenital, Hereditary, and Neonatal Diseases and Abnormalities | Finding | 69 | 11 | 0.100 | None | 0 |