AIP, aryl hydrocarbon receptor interacting protein, 9049
N. diseases: 216; N. variants: 24
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. | ||||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
phenotype | Finding | 18 | 0.100 | None | 0 | ||||||||||
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disease | Mental Disorders | Mental or Behavioral Dysfunction | 3 | 0.100 | None | 0 | |||||||||
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disease | Nervous System Diseases; Endocrine System Diseases | Disease or Syndrome | 48 | 0.100 | None | 0 | |||||||||
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phenotype | Finding | 5 | 0.100 | None | 0 | ||||||||||
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disease | Nervous System Diseases | Disease or Syndrome | 8 | 2 | 0.100 | None | 0 | ||||||||
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disease | Female Urogenital Diseases and Pregnancy Complications; Skin and Connective Tissue Diseases | Finding | 6 | 0.100 | None | 0 | |||||||||
|
disease | Endocrine System Diseases | Disease or Syndrome | 47 | 2 | 0.100 | None | 0 | ||||||||
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phenotype | Finding | 6 | 0.100 | None | 0 | ||||||||||
|
phenotype | Finding | 74 | 5 | 0.100 | None | 0 | |||||||||
|
phenotype | Finding | 77 | 11 | 0.100 | None | 0 | |||||||||
|
phenotype | Finding | 145 | 10 | 0.100 | None | 0 | |||||||||
|
phenotype | Finding | 71 | 10 | 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 | 133 | 13 | 0.100 | None | 0 | |||||||||
|
phenotype | Pathological Conditions, Signs and Symptoms; Skin and Connective Tissue Diseases | Finding | 113 | 3 | 0.100 | None | 0 | ||||||||
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phenotype | Finding | 19 | 3 | 0.100 | None | 0 | |||||||||
|
phenotype | Finding | 16 | 0.100 | None | 0 | ||||||||||
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phenotype | Finding | 23 | 8 | 0.100 | None | 0 | |||||||||
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phenotype | Finding | 19 | 6 | 0.100 | None | 0 | |||||||||
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disease | Musculoskeletal Diseases | Anatomical Abnormality | 35 | 0.100 | None | 0 | |||||||||
|
disease | Finding | 2 | 2 | 0.100 | None | 0 | 2 | ||||||||
|
phenotype | Finding | 103 | 4 | 0.100 | None | 0 | |||||||||
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phenotype | Musculoskeletal Diseases | Finding | 30 | 0.100 | None | 0 | |||||||||
|
phenotype | Finding | 2 | 0.100 | None | 0 | ||||||||||
|
disease | Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases | Congenital Abnormality | 30 | 0.100 | None | 0 |