AP3D1, adaptor related protein complex 3 subunit delta 1, 8943
N. diseases: 58; N. variants: 13
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. | ||||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
group | Nervous System Diseases | Disease or Syndrome | 977 | 39 | 0.010 | None | 1.000 | 1 | 2016 | 2016 | |||||
|
group | Infections | Disease or Syndrome | 108 | 10 | 0.010 | None | 1.000 | 1 | 2016 | 2016 | |||||
|
disease | Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Eye Diseases; Skin and Connective Tissue Diseases | Congenital Abnormality | 49 | 45 | 0.010 | None | 1.000 | 1 | 2019 | 2019 | |||||
|
disease | Nervous System Diseases | Disease or Syndrome | 1215 | 339 | 0.010 | None | 1.000 | 1 | 2019 | 2019 | |||||
|
phenotype | Pathological Conditions, Signs and Symptoms; Neoplasms | Neoplastic Process | 6243 | 355 | 0.010 | None | < 0.001 | 1 | 2003 | 2003 | |||||
|
group | Infections | Pathologic Function | 491 | 0.010 | None | 1.000 | 1 | 2008 | 2008 | ||||||
|
phenotype | Organism Attribute | 1903 | 3972 | 0.100 | None | 1.000 | 2 | 2 | 2019 | 2019 | |||||
|
phenotype | Laboratory Procedure | 717 | 1599 | 0.100 | None | 1.000 | 2 | 1 | 2016 | 2019 | |||||
|
phenotype | Laboratory Procedure | 131 | 224 | 0.100 | None | 1.000 | 1 | 1 | 2016 | 2016 | |||||
|
disease | Finding | 578 | 1158 | 0.100 | None | 1.000 | 1 | 1 | 2018 | 2018 | |||||
|
phenotype | Clinical Attribute | 144 | 211 | 0.100 | None | 1.000 | 1 | 1 | 2019 | 2019 | |||||
|
phenotype | Laboratory Procedure | 681 | 1322 | 0.100 | None | 1.000 | 1 | 1 | 2019 | 2019 | |||||
|
disease | Musculoskeletal Diseases | Anatomical Abnormality | 656 | 1178 | 0.100 | None | 1.000 | 1 | 1 | 2018 | 2018 | ||||
|
phenotype | Laboratory Procedure | 138 | 216 | 0.100 | None | 1.000 | 1 | 1 | 2016 | 2016 | |||||
|
phenotype | Organism Attribute | 565 | 1138 | 0.100 | None | 1.000 | 1 | 1 | 2019 | 2019 | |||||
|
phenotype | Laboratory or Test Result | 401 | 4389 | 0.100 | None | 1.000 | 1 | 4 | 2012 | 2012 | |||||
|
phenotype | Clinical Attribute | 843 | 1931 | 0.100 | None | 1.000 | 1 | 1 | 2019 | 2019 | |||||
|
disease | Pathological Conditions, Signs and Symptoms; Nervous System Diseases | Disease or Syndrome | 300 | 32 | 0.100 | None | 0 | ||||||||
|
disease | Congenital Abnormality | 489 | 64 | 0.100 | None | 0 | |||||||||
|
phenotype | Finding | 105 | 10 | 0.100 | None | 0 | |||||||||
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phenotype | Mental Disorders | Finding | 112 | 6 | 0.100 | None | 0 | ||||||||
|
phenotype | Finding | 779 | 0.100 | None | 0 | ||||||||||
|
phenotype | Finding | 11 | 0.100 | None | 0 | ||||||||||
|
disease | Pathological Conditions, Signs and Symptoms; Nervous System Diseases | Disease or Syndrome | 105 | 8 | 0.100 | None | 0 | ||||||||
|
phenotype | Infections; Respiratory Tract Diseases | Finding | 318 | 7 | 0.100 | None | 0 |