PIGO, phosphatidylinositol glycan anchor biosynthesis class O, 84720
N. diseases: 87; N. variants: 19
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. | ||||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
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disease | Disease or Syndrome | 1 | 15 | 0.600 | strong | 1.000 | 7 | 15 | 2012 | 2017 | |||||
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disease | Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Nervous System Diseases; Mental Disorders; Behavior and Behavior Mechanisms | Disease or Syndrome | 7 | 8 | 0.640 | None | 1.000 | 4 | 2 | 2012 | 2019 | ||||
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disease | Nervous System Diseases | Disease or Syndrome | 8 | 0.010 | None | 1.000 | 1 | 2013 | 2013 | ||||||
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phenotype | Anatomical Abnormality | 9 | 0.100 | None | 0 | ||||||||||
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phenotype | Finding | 11 | 1 | 0.100 | None | 0 | |||||||||
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phenotype | Finding | 11 | 1 | 0.100 | None | 0 | |||||||||
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phenotype | Finding | 13 | 0.100 | None | 0 | ||||||||||
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phenotype | Finding | 22 | 2 | 0.100 | None | 0 | |||||||||
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phenotype | Finding | 27 | 0.100 | None | 0 | ||||||||||
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phenotype | Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Digestive System Diseases | Finding | 28 | 1 | 0.100 | None | 0 | ||||||||
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disease | Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Cardiovascular Diseases | Congenital Abnormality | 28 | 5 | 0.100 | None | 0 | ||||||||
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phenotype | Finding | 29 | 6 | 0.100 | None | 0 | |||||||||
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phenotype | Finding | 30 | 0.100 | None | 0 | ||||||||||
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phenotype | Finding | 34 | 5 | 0.100 | None | 0 | |||||||||
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phenotype | Finding | 37 | 3 | 0.100 | None | 0 | |||||||||
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disease | Skin and Connective Tissue Diseases | Congenital Abnormality | 38 | 3 | 0.100 | None | 0 | ||||||||
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phenotype | Finding | 38 | 19 | 0.100 | None | 0 | |||||||||
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phenotype | Finding | 40 | 0.100 | None | 0 | ||||||||||
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disease | Cardiovascular Diseases | Finding | 43 | 0.100 | None | 0 | |||||||||
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phenotype | Congenital Abnormality | 45 | 7 | 0.100 | None | 0 | |||||||||
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phenotype | Finding | 48 | 14 | 0.100 | None | 0 | |||||||||
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phenotype | Nutritional and Metabolic Diseases; Musculoskeletal Diseases | Finding | 55 | 0.100 | None | 0 | |||||||||
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phenotype | Skin and Connective Tissue Diseases | Finding | 60 | 5 | 0.100 | None | 0 | ||||||||
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phenotype | Finding | 67 | 6 | 0.100 | None | 0 | |||||||||
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phenotype | Finding | 73 | 10 | 0.100 | None | 0 |