PIEZO2, piezo type mechanosensitive ion channel component 2, 63895
N. diseases: 224; N. variants: 30
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 | Musculoskeletal Diseases | Acquired Abnormality | 149 | 2 | 0.110 | None | 1.000 | 1 | 2019 | 2019 | |||||
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disease | Acquired Abnormality | 120 | 1 | 0.100 | None | 0 | |||||||||
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disease | Musculoskeletal Diseases | Acquired Abnormality | 5 | 0.100 | None | 0 | |||||||||
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disease | Musculoskeletal Diseases | Anatomical Abnormality | 111 | 12 | 0.010 | None | 1.000 | 1 | 2017 | 2017 | |||||
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disease | Anatomical Abnormality | 58 | 2 | 0.010 | None | 1.000 | 1 | 2019 | 2019 | ||||||
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disease | Musculoskeletal Diseases | Anatomical Abnormality | 155 | 17 | 0.110 | None | 1.000 | 1 | 2019 | 2019 | |||||
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disease | Anatomical Abnormality | 67 | 2 | 0.010 | None | 1.000 | 1 | 2019 | 2019 | ||||||
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phenotype | Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases | Anatomical Abnormality | 285 | 38 | 0.100 | None | 0 | ||||||||
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phenotype | Pathological Conditions, Signs and Symptoms | Anatomical Abnormality | 225 | 21 | 0.100 | None | 0 | ||||||||
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phenotype | Musculoskeletal Diseases | Anatomical Abnormality | 305 | 10 | 0.100 | None | 0 | ||||||||
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disease | Musculoskeletal Diseases | Anatomical Abnormality | 55 | 5 | 0.100 | None | 0 | ||||||||
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disease | Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases | Anatomical Abnormality | 72 | 2 | 0.100 | None | 0 | ||||||||
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disease | Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases | Anatomical Abnormality | 47 | 13 | 0.100 | None | 0 | ||||||||
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disease | Musculoskeletal Diseases | Anatomical Abnormality | 92 | 8 | 0.100 | None | 0 | ||||||||
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disease | Musculoskeletal Diseases; Wounds and Injuries | Anatomical Abnormality | 128 | 16 | 0.100 | None | 0 | ||||||||
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phenotype | Anatomical Abnormality | 46 | 11 | 0.100 | None | 0 | |||||||||
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disease | Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases; Stomatognathic Diseases | Anatomical Abnormality | 191 | 11 | 0.100 | None | 0 | ||||||||
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disease | Anatomical Abnormality | 9 | 0.100 | None | 0 | ||||||||||
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disease | Anatomical Abnormality | 10 | 2 | 0.100 | None | 0 | 2 | ||||||||
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disease | Anatomical Abnormality | 9 | 1 | 0.100 | None | 0 | |||||||||
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disease | Anatomical Abnormality | 6 | 0.100 | None | 0 | ||||||||||
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disease | Anatomical Abnormality | 16 | 0.100 | None | 0 | ||||||||||
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disease | Musculoskeletal Diseases | Anatomical Abnormality | 41 | 3 | 0.100 | None | 0 | ||||||||
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phenotype | Anatomical Abnormality | 16 | 2 | 0.100 | None | 0 | |||||||||
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phenotype | Clinical Attribute | 507 | 1037 | 0.100 | None | 1.000 | 1 | 1 | 2018 | 2018 |