ABCA12, ATP binding cassette subfamily A member 12, 26154
N. diseases: 85; N. variants: 27
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 | Finding | 112 | 9 | 0.100 | None | 0 | |||||||||
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disease | Finding | 24 | 5 | 0.100 | None | 0 | |||||||||
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phenotype | Finding | 22 | 0.100 | None | 0 | ||||||||||
|
phenotype | Finding | 52 | 0.100 | None | 0 | ||||||||||
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disease | Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Digestive System Diseases | Anatomical Abnormality | 17 | 0.100 | None | 0 | |||||||||
|
phenotype | Finding | 87 | 0.100 | None | 0 | ||||||||||
|
phenotype | Infections; Respiratory Tract Diseases | Finding | 318 | 7 | 0.100 | None | 0 | ||||||||
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phenotype | Finding | 6 | 2 | 0.100 | None | 0 | 2 | ||||||||
|
phenotype | Finding | 1010 | 0.100 | None | 0 | ||||||||||
|
phenotype | Finding | 137 | 0.100 | None | 0 | ||||||||||
|
phenotype | Finding | 84 | 3 | 0.100 | None | 0 | |||||||||
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phenotype | Finding | 21 | 2 | 0.100 | None | 0 | |||||||||
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phenotype | Finding | 105 | 3 | 0.100 | None | 0 | |||||||||
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phenotype | Finding | 39 | 3 | 0.100 | None | 0 | |||||||||
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phenotype | Finding | 117 | 1 | 0.100 | None | 0 | |||||||||
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disease | Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Skin and Connective Tissue Diseases | Disease or Syndrome | 165 | 19 | 0.100 | None | 0 | ||||||||
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disease | Pathological Conditions, Signs and Symptoms; Infections | Disease or Syndrome | 1453 | 144 | 0.100 | None | 0 | ||||||||
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disease | Eye Diseases | Acquired Abnormality | 878 | 124 | 0.100 | None | 0 | ||||||||
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disease | Pathological Conditions, Signs and Symptoms | Disease or Syndrome | 69 | 4 | 0.100 | None | 0 | ||||||||
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phenotype | Pathological Conditions, Signs and Symptoms; Cardiovascular Diseases | Pathologic Function | 133 | 40 | 0.100 | None | 0 | ||||||||
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phenotype | Behavior and Behavior Mechanisms | Mental or Behavioral Dysfunction | 91 | 9 | 0.100 | None | 0 | ||||||||
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phenotype | Pathological Conditions, Signs and Symptoms; Nutritional and Metabolic Diseases | Disease or Syndrome | 295 | 6 | 0.100 | None | 0 | ||||||||
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phenotype | Respiratory Tract Diseases | Pathologic Function | 315 | 15 | 0.100 | None | 0 | ||||||||
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disease | Skin and Connective Tissue Diseases | Disease or Syndrome | 69 | 1 | 0.100 | None | 0 | ||||||||
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phenotype | Pathological Conditions, Signs and Symptoms; Skin and Connective Tissue Diseases | Finding | 107 | 2 | 0.100 | None | 0 |