PPP1CB, protein phosphatase 1 catalytic subunit beta, 5500
N. diseases: 105; N. variants: 10
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 | Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases | Congenital Abnormality | 41 | 1 | 0.100 | None | 0 | ||||||||
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disease | Congenital Abnormality | 176 | 23 | 0.100 | None | 0 | |||||||||
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disease | Anatomical Abnormality | 30 | 0.100 | None | 0 | ||||||||||
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phenotype | Finding | 112 | 9 | 0.100 | None | 0 | |||||||||
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phenotype | Finding | 10 | 2 | 0.100 | None | 0 | |||||||||
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disease | Finding | 40 | 2 | 0.100 | None | 0 | |||||||||
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disease | Anatomical Abnormality | 12 | 1 | 0.100 | None | 0 | |||||||||
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phenotype | Finding | 1010 | 0.100 | None | 0 | ||||||||||
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disease | Cardiovascular Diseases | Disease or Syndrome | 106 | 40 | 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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phenotype | Finding | 223 | 19 | 0.100 | None | 0 | |||||||||
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phenotype | Finding | 85 | 7 | 0.100 | None | 0 | |||||||||
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phenotype | Finding | 86 | 11 | 0.100 | None | 0 | |||||||||
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phenotype | Finding | 265 | 23 | 0.100 | None | 0 | |||||||||
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phenotype | Finding | 22 | 10 | 0.100 | None | 0 | |||||||||
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phenotype | Finding | 407 | 35 | 0.100 | None | 0 | |||||||||
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phenotype | Finding | 42 | 5 | 0.100 | None | 0 | |||||||||
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phenotype | Finding | 145 | 10 | 0.100 | None | 0 | |||||||||
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phenotype | Finding | 46 | 7 | 0.100 | None | 0 | |||||||||
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phenotype | Finding | 42 | 1 | 0.100 | None | 0 | |||||||||
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phenotype | Finding | 159 | 25 | 0.100 | None | 0 | |||||||||
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phenotype | Finding | 52 | 0.100 | None | 0 | ||||||||||
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disease | Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Skin and Connective Tissue Diseases | Congenital Abnormality | 78 | 19 | 0.100 | None | 0 | ||||||||
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phenotype | Musculoskeletal Diseases | Pathologic Function | 224 | 15 | 0.100 | None | 0 | ||||||||
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disease | Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases | Disease or Syndrome | 488 | 90 | 0.100 | None | 0 |