KCNJ2, potassium inwardly rectifying channel subfamily J member 2, 3759
N. diseases: 117; N. variants: 33
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 Abnormality | 62 | 34 | 0.100 | None | 0 | |||||||||
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phenotype | Pathological Conditions, Signs and Symptoms | Finding | 109 | 13 | 0.100 | None | 0 | ||||||||
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phenotype | Finding | 116 | 0.100 | None | 0 | ||||||||||
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phenotype | Finding | 108 | 31 | 0.100 | None | 0 | |||||||||
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phenotype | Finding | 295 | 14 | 0.100 | None | 0 | |||||||||
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phenotype | Pathological Conditions, Signs and Symptoms; Cardiovascular Diseases | Finding | 63 | 2 | 0.100 | None | 0 | ||||||||
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phenotype | Finding | 91 | 16 | 0.100 | None | 0 | |||||||||
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phenotype | Finding | 41 | 1 | 0.100 | None | 0 | |||||||||
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disease | Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Skin and Connective Tissue Diseases | Congenital Abnormality | 40 | 5 | 0.100 | None | 0 | ||||||||
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phenotype | Disease or Syndrome | 12 | 1 | 0.100 | None | 0 | |||||||||
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disease | Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases | Congenital Abnormality | 129 | 11 | 0.100 | None | 0 | ||||||||
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phenotype | Finding | 49 | 5 | 0.100 | None | 0 | |||||||||
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phenotype | Finding | 73 | 3 | 0.100 | None | 0 | |||||||||
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disease | Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases; Nervous System Diseases; Stomatognathic Diseases | Congenital Abnormality | 497 | 70 | 0.100 | None | 0 | ||||||||
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phenotype | Finding | 123 | 13 | 0.100 | None | 0 | |||||||||
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disease | Congenital Abnormality | 113 | 5 | 0.100 | None | 0 | |||||||||
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disease | Congenital Abnormality | 489 | 64 | 0.100 | None | 0 | |||||||||
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disease | Pathological Conditions, Signs and Symptoms; Cardiovascular Diseases | Disease or Syndrome | 226 | 8 | 0.100 | None | 0 | ||||||||
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phenotype | Finding | 35 | 5 | 0.100 | None | 0 | |||||||||
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phenotype | Finding | 111 | 16 | 0.100 | None | 0 | |||||||||
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disease | Anatomical Abnormality | 13 | 4 | 0.100 | None | 0 | |||||||||
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disease | Disease or Syndrome | 9 | 0.100 | None | 0 | ||||||||||
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phenotype | Finding | 64 | 0.100 | None | 0 | ||||||||||
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phenotype | Finding | 1 | 0.100 | None | 0 | ||||||||||
|
phenotype | Finding | 3 | 0.100 | None | 0 |