MGAT2, alpha-1,6-mannosyl-glycoprotein 2-beta-N-acetylglucosaminyltransferase, 4247
N. diseases: 76; N. variants: 9
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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phenotype | Pathological Conditions, Signs and Symptoms; Nervous System Diseases | Finding | 955 | 164 | 0.100 | None | 0 | ||||||||
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phenotype | Finding | 391 | 49 | 0.100 | None | 0 | |||||||||
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phenotype | Stomatognathic Diseases | Finding | 100 | 5 | 0.100 | None | 0 | ||||||||
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phenotype | Finding | 1127 | 292 | 0.100 | None | 0 | |||||||||
|
phenotype | Finding | 32 | 3 | 0.100 | None | 0 | |||||||||
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disease | Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Hemic and Lymphatic Diseases | Disease or Syndrome | 27 | 52 | 0.100 | None | 0 | ||||||||
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disease | Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Stomatognathic Diseases | Congenital Abnormality | 12 | 1 | 0.100 | None | 0 | ||||||||
|
phenotype | Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Stomatognathic Diseases | Finding | 140 | 16 | 0.100 | None | 0 | ||||||||
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phenotype | Finding | 27 | 4 | 0.100 | None | 0 | |||||||||
|
phenotype | Finding | 79 | 14 | 0.100 | None | 0 | |||||||||
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phenotype | Finding | 96 | 11 | 0.100 | None | 0 | |||||||||
|
phenotype | Pathological Conditions, Signs and Symptoms; Musculoskeletal Diseases | Finding | 68 | 5 | 0.100 | None | 0 | ||||||||
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phenotype | Pathological Conditions, Signs and Symptoms; Nervous System Diseases | Finding | 143 | 14 | 0.100 | None | 0 | ||||||||
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phenotype | Finding | 271 | 106 | 0.100 | None | 0 | 1 | ||||||||
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disease | Congenital Abnormality | 176 | 23 | 0.100 | None | 0 | |||||||||
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phenotype | Finding | 17 | 1 | 0.100 | None | 0 | |||||||||
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phenotype | Finding | 180 | 8 | 0.100 | None | 0 | |||||||||
|
phenotype | Finding | 83 | 17 | 0.100 | None | 0 | |||||||||
|
phenotype | Finding | 104 | 13 | 0.100 | None | 0 | |||||||||
|
phenotype | Finding | 105 | 3 | 0.100 | None | 0 | |||||||||
|
phenotype | Pathological Conditions, Signs and Symptoms; Nervous System Diseases; Mental Disorders; Behavior and Behavior Mechanisms | Finding | 45 | 1 | 0.100 | None | 0 | ||||||||
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phenotype | Finding | 35 | 5 | 0.100 | None | 0 | |||||||||
|
phenotype | Finding | 6 | 0.100 | None | 0 | ||||||||||
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phenotype | Finding | 2 | 1 | 0.100 | None | 0 | |||||||||
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disease | Mental or Behavioral Dysfunction | 1825 | 553 | 0.100 | None | 0 | 1 |