PIGL, phosphatidylinositol glycan anchor biosynthesis class L, 9487
N. diseases: 152; N. variants: 11
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 | 35 | 7 | 0.100 | None | 0 | |||||||||
|
disease | Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Cardiovascular Diseases | Congenital Abnormality | 28 | 5 | 0.100 | None | 0 | ||||||||
|
phenotype | Finding | 426 | 39 | 0.100 | None | 0 | |||||||||
|
phenotype | Finding | 95 | 15 | 0.100 | None | 0 | |||||||||
|
phenotype | Finding | 9 | 2 | 0.100 | None | 0 | |||||||||
|
phenotype | Finding | 159 | 25 | 0.100 | None | 0 | |||||||||
|
phenotype | Finding | 46 | 7 | 0.100 | None | 0 | |||||||||
|
phenotype | Finding | 37 | 3 | 0.100 | None | 0 | |||||||||
|
phenotype | Finding | 112 | 9 | 0.100 | None | 0 | |||||||||
|
phenotype | Finding | 34 | 5 | 0.100 | None | 0 | |||||||||
|
phenotype | Finding | 145 | 10 | 0.100 | None | 0 | |||||||||
|
phenotype | Finding | 79 | 8 | 0.100 | None | 0 | |||||||||
|
phenotype | Finding | 117 | 1 | 0.100 | None | 0 | |||||||||
|
phenotype | Finding | 110 | 13 | 0.100 | None | 0 | |||||||||
|
phenotype | Finding | 71 | 10 | 0.100 | None | 0 | |||||||||
|
phenotype | Congenital Abnormality | 45 | 7 | 0.100 | None | 0 | |||||||||
|
phenotype | Pathological Conditions, Signs and Symptoms | Finding | 194 | 33 | 0.100 | None | 0 | ||||||||
|
phenotype | Pathological Conditions, Signs and Symptoms; Nervous System Diseases; Otorhinolaryngologic Diseases | Disease or Syndrome | 740 | 337 | 0.100 | None | 0 | ||||||||
|
disease | Musculoskeletal Diseases; Wounds and Injuries | Anatomical Abnormality | 128 | 16 | 0.100 | None | 0 | ||||||||
|
disease | Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Skin and Connective Tissue Diseases | Congenital Abnormality | 44 | 0.100 | None | 0 | |||||||||
|
disease | Congenital Abnormality | 33 | 1 | 0.100 | None | 0 | |||||||||
|
phenotype | Pathologic Function | 244 | 40 | 0.100 | None | 0 | |||||||||
|
disease | Pathological Conditions, Signs and Symptoms; Nervous System Diseases | Disease or Syndrome | 300 | 32 | 0.100 | None | 0 | ||||||||
|
phenotype | Finding | 288 | 29 | 0.100 | None | 0 | |||||||||
|
phenotype | Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases | Pathologic Function | 14 | 2 | 0.100 | None | 0 |