PACS1, phosphofurin acidic cluster sorting protein 1, 55690
N. diseases: 109; N. variants: 7
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 | 211 | 25 | 0.100 | None | 0 | |||||||||
|
phenotype | Eye Diseases | Finding | 50 | 14 | 0.100 | None | 0 | ||||||||
|
phenotype | Anatomical Abnormality | 122 | 14 | 0.100 | None | 0 | |||||||||
|
phenotype | Finding | 141 | 14 | 0.100 | None | 0 | |||||||||
|
phenotype | Finding | 779 | 0.100 | None | 0 | ||||||||||
|
disease | Mental or Behavioral Dysfunction | 7 | 4 | 0.100 | None | 0 | |||||||||
|
disease | Finding | 6 | 5 | 0.100 | None | 0 | 1 | ||||||||
|
disease | Congenital Abnormality | 2 | 0.100 | None | 0 | ||||||||||
|
disease | Behavior and Behavior Mechanisms | Mental or Behavioral Dysfunction | 4 | 0.100 | None | 0 | |||||||||
|
disease | Congenital Abnormality | 35 | 3 | 0.100 | None | 0 | |||||||||
|
phenotype | Neoplasms | Finding | 9 | 2 | 0.100 | None | 0 | 1 | |||||||
|
phenotype | Pathological Conditions, Signs and Symptoms; Nervous System Diseases | Finding | 118 | 24 | 0.100 | None | 0 | ||||||||
|
phenotype | Finding | 12 | 0.100 | None | 0 | ||||||||||
|
phenotype | Finding | 17 | 2 | 0.100 | None | 0 | |||||||||
|
phenotype | Finding | 71 | 17 | 0.100 | None | 0 | |||||||||
|
phenotype | Finding | 71 | 10 | 0.100 | None | 0 | 1 | ||||||||
|
disease | Congenital Abnormality | 284 | 39 | 0.100 | None | 0 | |||||||||
|
phenotype | Finding | 83 | 17 | 0.100 | None | 0 | |||||||||
|
phenotype | Pathological Conditions, Signs and Symptoms; Nervous System Diseases | Finding | 232 | 72 | 0.100 | None | 0 | ||||||||
|
phenotype | Finding | 152 | 6 | 0.100 | None | 0 | |||||||||
|
phenotype | Finding | 20 | 5 | 0.100 | None | 0 | |||||||||
|
phenotype | Pathological Conditions, Signs and Symptoms; Nervous System Diseases | Finding | 955 | 164 | 0.100 | None | 0 | ||||||||
|
phenotype | Finding | 779 | 0.100 | None | 0 | ||||||||||
|
disease | Musculoskeletal Diseases | Disease or Syndrome | 850 | 135 | 0.100 | None | 0 | ||||||||
|
disease | Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Cardiovascular Diseases | Congenital Abnormality | 510 | 56 | 0.100 | None | 0 |