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. | ||||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
disease | Congenital Abnormality | 417 | 30 | 0.100 | None | 0 | |||||||||
|
phenotype | Congenital Abnormality | 18 | 1 | 0.100 | None | 0 | |||||||||
|
phenotype | Finding | 391 | 49 | 0.100 | None | 0 | |||||||||
|
phenotype | Finding | 216 | 16 | 0.100 | None | 0 | |||||||||
|
phenotype | Finding | 168 | 7 | 0.100 | None | 0 | |||||||||
|
phenotype | Stomatognathic Diseases | Finding | 100 | 5 | 0.100 | None | 0 | ||||||||
|
phenotype | Finding | 1127 | 292 | 0.100 | None | 0 | |||||||||
|
phenotype | Finding | 41 | 0.100 | None | 0 | ||||||||||
|
disease | Otorhinolaryngologic Diseases | Disease or Syndrome | 163 | 6 | 0.100 | None | 0 | ||||||||
|
phenotype | Congenital, Hereditary, and Neonatal Diseases and Abnormalities | Finding | 69 | 11 | 0.100 | None | 0 | ||||||||
|
phenotype | Finding | 67 | 11 | 0.100 | None | 0 | |||||||||
|
disease | Congenital Abnormality | 176 | 23 | 0.100 | None | 0 | |||||||||
|
phenotype | Finding | 116 | 0.100 | None | 0 | ||||||||||
|
phenotype | Finding | 108 | 31 | 0.100 | None | 0 | |||||||||
|
phenotype | Finding | 35 | 3 | 0.100 | None | 0 | |||||||||
|
disease | Mental or Behavioral Dysfunction | 1825 | 553 | 0.100 | None | 0 | |||||||||
|
phenotype | Finding | 295 | 14 | 0.100 | None | 0 | |||||||||
|
phenotype | Finding | 288 | 29 | 0.100 | None | 0 | |||||||||
|
disease | Musculoskeletal Diseases | Congenital Abnormality | 40 | 6 | 0.100 | None | 0 | ||||||||
|
disease | Congenital Abnormality | 2 | 1 | 0.100 | None | 0 | |||||||||
|
disease | Congenital, Hereditary, and Neonatal Diseases and Abnormalities | Congenital Abnormality | 237 | 0.100 | None | 0 | |||||||||
|
phenotype | Finding | 73 | 10 | 0.100 | None | 0 | |||||||||
|
disease | Congenital Abnormality | 148 | 18 | 0.100 | None | 0 | |||||||||
|
phenotype | Infections; Respiratory Tract Diseases | Finding | 318 | 7 | 0.100 | None | 0 | ||||||||
|
group | Pathological Conditions, Signs and Symptoms; Nervous System Diseases; Mental Disorders; Behavior and Behavior Mechanisms | Mental or Behavioral Dysfunction | 2165 | 159 | 0.100 | None | 0 |