DYRK1A, dual specificity tyrosine phosphorylation regulated kinase 1A, 1859
N. diseases: 212; N. variants: 55
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 | 1127 | 292 | 0.100 | None | 1.000 | 1 | 10 | 2015 | 2015 | |||||
|
phenotype | Pathologic Function | 41 | 56 | 0.100 | None | 1.000 | 1 | 8 | 2015 | 2015 | |||||
|
phenotype | Laboratory Procedure | 681 | 1322 | 0.100 | None | 1.000 | 1 | 1 | 2019 | 2019 | |||||
|
phenotype | Finding | 653 | 1206 | 0.100 | None | 1.000 | 1 | 1 | 2019 | 2019 | |||||
|
phenotype | Finding | 211 | 411 | 0.100 | None | 1.000 | 1 | 17 | 2015 | 2015 | |||||
|
phenotype | Finding | 75 | 24 | 0.100 | None | 1.000 | 1 | 6 | 2015 | 2015 | |||||
|
disease | Finding | 578 | 1158 | 0.100 | None | 1.000 | 1 | 1 | 2018 | 2018 | |||||
|
phenotype | Finding | 160 | 246 | 0.100 | None | 1.000 | 1 | 17 | 2015 | 2015 | |||||
|
phenotype | Finding | 1 | 9 | 0.100 | None | 1.000 | 1 | 9 | 2015 | 2015 | |||||
|
disease | Musculoskeletal Diseases | Anatomical Abnormality | 656 | 1178 | 0.100 | None | 1.000 | 1 | 1 | 2018 | 2018 | ||||
|
phenotype | Finding | 89 | 11 | 0.100 | None | 0 | |||||||||
|
phenotype | Finding | 8 | 1 | 0.100 | None | 0 | 1 | ||||||||
|
phenotype | Congenital Abnormality | 79 | 8 | 0.100 | None | 0 | 1 | ||||||||
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disease | Congenital Abnormality | 5 | 1 | 0.100 | None | 0 | 1 | ||||||||
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phenotype | Finding | 111 | 16 | 0.100 | None | 0 | 1 | ||||||||
|
phenotype | Pathological Conditions, Signs and Symptoms; Eye Diseases; Nervous System Diseases | Finding | 171 | 54 | 0.100 | None | 0 | 9 | |||||||
|
phenotype | Finding | 271 | 106 | 0.100 | None | 0 | 1 | ||||||||
|
phenotype | Finding | 159 | 25 | 0.100 | None | 0 | 1 | ||||||||
|
phenotype | Finding | 130 | 50 | 0.100 | None | 0 | |||||||||
|
phenotype | Pathological Conditions, Signs and Symptoms; Nervous System Diseases | Finding | 59 | 4 | 0.100 | None | 0 | ||||||||
|
disease | Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases | Congenital Abnormality | 127 | 83 | 0.100 | None | 0 | 1 | |||||||
|
phenotype | Behavior and Behavior Mechanisms | Finding | 560 | 192 | 0.100 | None | 0 | 2 | |||||||
|
phenotype | Finding | 108 | 31 | 0.100 | None | 0 | 1 | ||||||||
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disease | Mental or Behavioral Dysfunction | 9 | 5 | 0.100 | None | 0 | 1 | ||||||||
|
phenotype | Anatomical Abnormality | 3 | 4 | 0.100 | None | 0 | 1 |