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 | Musculoskeletal Diseases | Disease or Syndrome | 20 | 17 | 0.100 | None | 0 | ||||||||
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phenotype | Finding | 216 | 16 | 0.100 | None | 0 | |||||||||
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disease | Congenital Abnormality | 417 | 30 | 0.100 | None | 0 | |||||||||
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phenotype | Finding | 116 | 0.100 | None | 0 | ||||||||||
|
phenotype | Finding | 108 | 31 | 0.100 | None | 0 | |||||||||
|
phenotype | Finding | 35 | 3 | 0.100 | None | 0 | |||||||||
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disease | Mental or Behavioral Dysfunction | 1825 | 553 | 0.100 | None | 0 | |||||||||
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phenotype | Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Eye Diseases | Finding | 70 | 13 | 0.100 | None | 0 | ||||||||
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phenotype | Finding | 1127 | 292 | 0.100 | None | 0 | |||||||||
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disease | Congenital Abnormality | 148 | 18 | 0.100 | None | 0 | |||||||||
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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 | ||||||||
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disease | Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases | Disease or Syndrome | 121 | 11 | 0.100 | None | 0 | ||||||||
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disease | Anatomical Abnormality | 67 | 2 | 0.100 | None | 0 | |||||||||
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disease | Finding | 40 | 0.100 | None | 0 | ||||||||||
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phenotype | Finding | 1010 | 0.100 | None | 0 | ||||||||||
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phenotype | Finding | 3 | 2 | 0.100 | None | 0 | |||||||||
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phenotype | Anatomical Abnormality | 122 | 14 | 0.100 | None | 0 | |||||||||
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phenotype | Finding | 71 | 5 | 0.100 | None | 0 | |||||||||
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phenotype | Finding | 11 | 2 | 0.100 | None | 0 | |||||||||
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phenotype | Infections; Respiratory Tract Diseases | Finding | 318 | 7 | 0.100 | None | 0 | ||||||||
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disease | Disease or Syndrome | 11 | 0.100 | None | 0 | ||||||||||
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phenotype | Finding | 4 | 0.100 | None | 0 | ||||||||||
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disease | Anatomical Abnormality | 29 | 1 | 0.100 | None | 0 | |||||||||
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disease | Anatomical Abnormality | 11 | 1 | 0.100 | None | 0 | |||||||||
|
disease | Anatomical Abnormality | 3 | 1 | 0.100 | None | 0 |