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 | Mental or Behavioral Dysfunction | 1825 | 553 | 0.100 | None | 0 | |||||||||
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group | Pathological Conditions, Signs and Symptoms; Nervous System Diseases | Finding | 312 | 23 | 0.100 | None | 0 | ||||||||
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phenotype | Musculoskeletal Diseases | Finding | 19 | 3 | 0.100 | None | 0 | ||||||||
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phenotype | Finding | 116 | 0.100 | None | 0 | ||||||||||
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disease | Congenital Abnormality | 417 | 30 | 0.100 | None | 0 | |||||||||
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disease | Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases | Congenital Abnormality | 123 | 10 | 0.100 | None | 0 | ||||||||
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phenotype | Finding | 75 | 24 | 0.100 | None | 0 | |||||||||
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disease | Behavior and Behavior Mechanisms | Mental or Behavioral Dysfunction | 261 | 78 | 0.100 | None | 0 | ||||||||
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disease | Pathological Conditions, Signs and Symptoms; Skin and Connective Tissue Diseases | Disease or Syndrome | 176 | 19 | 0.100 | None | 0 | ||||||||
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phenotype | Finding | 67 | 6 | 0.100 | None | 0 | |||||||||
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disease | Anatomical Abnormality | 95 | 8 | 0.100 | None | 0 | |||||||||
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phenotype | Pathological Conditions, Signs and Symptoms; Female Urogenital Diseases and Pregnancy Complications | Finding | 43 | 10 | 0.100 | None | 0 | ||||||||
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phenotype | Finding | 3 | 0.100 | None | 0 | ||||||||||
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group | Pathological Conditions, Signs and Symptoms; Nervous System Diseases; Mental Disorders; Behavior and Behavior Mechanisms | Mental or Behavioral Dysfunction | 2165 | 159 | 0.100 | None | 0 | ||||||||
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disease | Anatomical Abnormality | 30 | 0.100 | None | 0 | ||||||||||
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phenotype | Finding | 40 | 0.100 | None | 0 | ||||||||||
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phenotype | Anatomical Abnormality | 86 | 0.100 | None | 0 | ||||||||||
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phenotype | Finding | 30 | 0.100 | None | 0 | ||||||||||
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phenotype | Anatomical Abnormality | 9 | 0.100 | None | 0 | ||||||||||
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phenotype | Anatomical Abnormality | 1 | 0.100 | None | 0 | ||||||||||
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phenotype | Finding | 38 | 19 | 0.100 | None | 0 | |||||||||
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phenotype | Finding | 3 | 0.100 | None | 0 | ||||||||||
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phenotype | Finding | 11 | 1 | 0.100 | None | 0 | |||||||||
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disease | Congenital Abnormality | 148 | 18 | 0.100 | None | 0 | |||||||||
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disease | Congenital Abnormality | 97 | 7 | 0.100 | None | 0 |