INPPL1, inositol polyphosphate phosphatase like 1, 3636
N. diseases: 133; N. variants: 16
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 | 14 | 0.100 | None | 0 | ||||||||||
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phenotype | Finding | 112 | 18 | 0.100 | None | 0 | |||||||||
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phenotype | Finding | 116 | 0.100 | None | 0 | ||||||||||
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phenotype | Finding | 16 | 0.100 | None | 0 | ||||||||||
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phenotype | Finding | 14 | 0.100 | None | 0 | ||||||||||
|
phenotype | Finding | 426 | 39 | 0.100 | None | 0 | |||||||||
|
phenotype | Finding | 13 | 0.100 | None | 0 | ||||||||||
|
phenotype | Finding | 42 | 1 | 0.100 | None | 0 | |||||||||
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phenotype | Finding | 45 | 6 | 0.100 | None | 0 | |||||||||
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disease | Congenital Abnormality | 154 | 26 | 0.100 | None | 0 | |||||||||
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disease | Hemic and Lymphatic Diseases | Pathologic Function | 61 | 1 | 0.100 | None | 0 | ||||||||
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disease | Anatomical Abnormality | 97 | 0.100 | None | 0 | ||||||||||
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phenotype | Finding | 14 | 0.100 | None | 0 | ||||||||||
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disease | Anatomical Abnormality | 190 | 12 | 0.100 | None | 0 | |||||||||
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phenotype | Finding | 16 | 0.100 | None | 0 | ||||||||||
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phenotype | Finding | 11 | 0.100 | None | 0 | ||||||||||
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phenotype | Finding | 282 | 16 | 0.100 | None | 0 | |||||||||
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phenotype | Finding | 10 | 0.100 | None | 0 | ||||||||||
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disease | Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Male Urogenital Diseases; Endocrine System Diseases | Congenital Abnormality | 725 | 80 | 0.100 | None | 0 | ||||||||
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phenotype | Finding | 26 | 7 | 0.100 | None | 0 | |||||||||
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phenotype | Pathological Conditions, Signs and Symptoms; Nervous System Diseases | Finding | 955 | 164 | 0.100 | None | 0 | ||||||||
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disease | Congenital Abnormality | 57 | 6 | 0.100 | None | 0 | |||||||||
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disease | Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases; Stomatognathic Diseases | Congenital Abnormality | 611 | 158 | 0.100 | None | 0 | ||||||||
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phenotype | Finding | 4 | 0.100 | None | 0 | ||||||||||
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phenotype | Infections; Respiratory Tract Diseases | Finding | 318 | 7 | 0.100 | None | 0 |