AUTS2, activator of transcription and developmental regulator AUTS2, 26053
N. diseases: 149; N. variants: 57
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 | Pathological Conditions, Signs and Symptoms | Disease or Syndrome | 32 | 35 | 0.100 | None | 1.000 | 1 | 1 | 2015 | 2015 | ||||
|
phenotype | Finding | 653 | 1206 | 0.100 | None | 1.000 | 1 | 1 | 2019 | 2019 | |||||
|
disease | Mental Disorders | Mental or Behavioral Dysfunction | 1236 | 1451 | 0.100 | None | 1.000 | 1 | 1 | 2015 | 2015 | ||||
|
phenotype | Clinical Attribute | 843 | 1931 | 0.100 | None | 1.000 | 1 | 1 | 2019 | 2019 | |||||
|
phenotype | Clinical Attribute | 430 | 746 | 0.100 | None | 1.000 | 1 | 1 | 2019 | 2019 | |||||
|
phenotype | Finding | 2 | 2 | 0.100 | None | 1.000 | 1 | 1 | 2012 | 2012 | |||||
|
disease | Pathological Conditions, Signs and Symptoms; Skin and Connective Tissue Diseases | Disease or Syndrome | 491 | 375 | 0.100 | None | 1.000 | 1 | 3 | 2017 | 2017 | ||||
|
phenotype | Organism Attribute | 1903 | 3972 | 0.100 | None | 1.000 | 1 | 2 | 2019 | 2019 | |||||
|
phenotype | Cell Function | 28 | 53 | 0.100 | None | 1.000 | 1 | 1 | 2015 | 2015 | |||||
|
phenotype | Laboratory Procedure | 717 | 1599 | 0.100 | None | 1.000 | 1 | 1 | 2019 | 2019 | |||||
|
disease | Neoplasms | Neoplastic Process | 3111 | 6892 | 0.100 | None | 1.000 | 1 | 12 | 2017 | 2017 | ||||
|
phenotype | Behavior and Behavior Mechanisms | Individual Behavior | 210 | 535 | 0.100 | None | 1.000 | 1 | 1 | 2011 | 2011 | ||||
|
disease | Congenital Abnormality | 62 | 34 | 0.100 | None | 0 | 1 | ||||||||
|
disease | Behavior and Behavior Mechanisms | Mental or Behavioral Dysfunction | 261 | 78 | 0.100 | None | 0 | ||||||||
|
phenotype | Finding | 11 | 15 | 0.100 | None | 0 | 1 | ||||||||
|
phenotype | Finding | 24 | 28 | 0.100 | None | 0 | 1 | ||||||||
|
phenotype | Finding | 129 | 21 | 0.100 | None | 0 | 1 | ||||||||
|
disease | Congenital Abnormality | 5 | 1 | 0.100 | None | 0 | |||||||||
|
disease | Congenital Abnormality | 417 | 30 | 0.100 | None | 0 | |||||||||
|
disease | Musculoskeletal Diseases | Anatomical Abnormality | 117 | 5 | 0.100 | None | 0 | 1 | |||||||
|
phenotype | Finding | 477 | 0.100 | None | 0 | ||||||||||
|
phenotype | Disease or Syndrome | 30 | 25 | 0.100 | None | 0 | 1 | ||||||||
|
disease | Mental or Behavioral Dysfunction | 9 | 5 | 0.100 | None | 0 | 1 | ||||||||
|
phenotype | Behavior and Behavior Mechanisms | Finding | 560 | 192 | 0.100 | None | 0 | ||||||||
|
disease | Respiratory Tract Diseases; Nervous System Diseases | Disease or Syndrome | 480 | 105 | 0.100 | None | 0 | 1 |