KANSL1, KAT8 regulatory NSL complex subunit 1, 284058
N. diseases: 140; N. variants: 332
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 | 16 | 8 | 0.100 | None | 0 | |||||||||
|
phenotype | Finding | 182 | 12 | 0.100 | None | 0 | |||||||||
|
phenotype | Finding | 129 | 21 | 0.100 | None | 0 | |||||||||
|
phenotype | Finding | 46 | 7 | 0.100 | None | 0 | |||||||||
|
phenotype | Finding | 111 | 0.100 | None | 0 | ||||||||||
|
disease | Disease or Syndrome | 2 | 0.100 | None | 0 | ||||||||||
|
phenotype | Finding | 211 | 411 | 0.100 | None | 0 | 1 | ||||||||
|
phenotype | Finding | 71 | 10 | 0.100 | None | 0 | 1 | ||||||||
|
phenotype | Pathological Conditions, Signs and Symptoms; Nervous System Diseases | Finding | 208 | 9 | 0.100 | None | 0 | ||||||||
|
phenotype | Finding | 105 | 3 | 0.100 | None | 0 | |||||||||
|
phenotype | Finding | 96 | 19 | 0.100 | None | 0 | |||||||||
|
disease | Musculoskeletal Diseases | Anatomical Abnormality | 26 | 7 | 0.100 | None | 0 | 1 | |||||||
|
phenotype | Finding | 17 | 0.100 | None | 0 | ||||||||||
|
disease | Congenital Abnormality | 417 | 30 | 0.100 | None | 0 | 1 | ||||||||
|
phenotype | Finding | 20 | 5 | 0.100 | None | 0 | |||||||||
|
phenotype | Finding | 7 | 0.100 | None | 0 | ||||||||||
|
disease | Disease or Syndrome | 52 | 0.100 | None | 0 | ||||||||||
|
phenotype | Finding | 180 | 8 | 0.100 | None | 0 | |||||||||
|
phenotype | Finding | 3 | 2 | 0.100 | None | 0 | |||||||||
|
disease | Musculoskeletal Diseases; Wounds and Injuries | Anatomical Abnormality | 128 | 16 | 0.100 | None | 0 | ||||||||
|
phenotype | Finding | 40 | 5 | 0.100 | None | 0 | |||||||||
|
phenotype | Finding | 133 | 13 | 0.100 | None | 0 | |||||||||
|
disease | Behavior and Behavior Mechanisms | Mental or Behavioral Dysfunction | 1048 | 287 | 0.100 | None | 0 | ||||||||
|
disease | Pathological Conditions, Signs and Symptoms | Disease or Syndrome | 842 | 10 | 0.100 | None | 0 | ||||||||
|
phenotype | Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Female Urogenital Diseases and Pregnancy Complications | Disease or Syndrome | 1037 | 21 | 0.100 | None | 0 |