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. | ||||
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disease | Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Eye Diseases; Skin and Connective Tissue Diseases; Nervous System Diseases; Mental Disorders; Otorhinolaryngologic Diseases; Behavior and Behavior Mechanisms; Cardiovascular Diseases | Disease or Syndrome | 1 | 4 | 0.730 | None | 1.000 | 4 | 4 | 2012 | 2019 | ||||
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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 | 0.300 | None | 1.000 | 1 | 2015 | 2015 | |||||
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phenotype | Laboratory Procedure | 681 | 1322 | 0.100 | None | 1.000 | 2 | 2 | 2016 | 2019 | |||||
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disease | Nutritional and Metabolic Diseases; Nervous System Diseases | Disease or Syndrome | 1114 | 485 | 0.100 | None | 1.000 | 2 | 1 | 2013 | 2014 | ||||
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phenotype | Laboratory Procedure | 610 | 1144 | 0.100 | None | 1.000 | 1 | 1 | 2016 | 2016 | |||||
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phenotype | Clinical Attribute | 507 | 1037 | 0.100 | None | 1.000 | 1 | 1 | 2017 | 2017 | |||||
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phenotype | Laboratory Procedure | 272 | 452 | 0.100 | None | 1.000 | 1 | 1 | 2016 | 2016 | |||||
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phenotype | Mental Process | 854 | 2127 | 0.100 | None | 1.000 | 1 | 1 | 2018 | 2018 | |||||
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phenotype | Laboratory Procedure | 100 | 150 | 0.100 | None | 1.000 | 1 | 1 | 2016 | 2016 | |||||
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phenotype | Laboratory Procedure | 145 | 234 | 0.100 | None | 1.000 | 1 | 2 | 2016 | 2016 | |||||
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phenotype | Clinical Attribute | 430 | 746 | 0.100 | None | 1.000 | 1 | 1 | 2019 | 2019 | |||||
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phenotype | Finding | 34 | 5 | 0.100 | None | 0 | |||||||||
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phenotype | Finding | 112 | 9 | 0.100 | None | 0 | |||||||||
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phenotype | Finding | 37 | 3 | 0.100 | None | 0 | |||||||||
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phenotype | Finding | 46 | 7 | 0.100 | None | 0 | |||||||||
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phenotype | Finding | 145 | 10 | 0.100 | None | 0 | |||||||||
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phenotype | Finding | 117 | 1 | 0.100 | None | 0 | |||||||||
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phenotype | Finding | 79 | 8 | 0.100 | None | 0 | |||||||||
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disease | Anatomical Abnormality | 95 | 8 | 0.100 | None | 0 | |||||||||
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phenotype | Finding | 110 | 13 | 0.100 | None | 0 | |||||||||
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phenotype | Finding | 71 | 10 | 0.100 | None | 0 | |||||||||
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phenotype | Congenital Abnormality | 45 | 7 | 0.100 | None | 0 | |||||||||
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phenotype | Pathological Conditions, Signs and Symptoms | Finding | 194 | 33 | 0.100 | None | 0 | ||||||||
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phenotype | Finding | 159 | 25 | 0.100 | None | 0 | |||||||||
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phenotype | Finding | 9 | 2 | 0.100 | None | 0 |