KCNJ6, potassium inwardly rectifying channel subfamily J member 6, 3763
N. diseases: 104; N. variants: 110
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 | 129 | 0.100 | None | 0 | ||||||||||
|
disease | Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases; Nervous System Diseases; Stomatognathic Diseases | Congenital Abnormality | 497 | 70 | 0.100 | None | 0 | ||||||||
|
disease | Finding | 16 | 3 | 0.100 | None | 0 | |||||||||
|
phenotype | Finding | 47 | 2 | 0.100 | None | 0 | |||||||||
|
phenotype | Finding | 42 | 5 | 0.100 | None | 0 | |||||||||
|
phenotype | Finding | 12 | 1 | 0.100 | None | 0 | |||||||||
|
disease | Musculoskeletal Diseases | Disease or Syndrome | 850 | 135 | 0.100 | None | 0 | ||||||||
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phenotype | Respiratory Tract Diseases | Pathologic Function | 315 | 15 | 0.100 | None | 0 | ||||||||
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phenotype | Congenital Abnormality | 79 | 8 | 0.100 | None | 0 | |||||||||
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phenotype | Finding | 130 | 50 | 0.100 | None | 0 | |||||||||
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phenotype | Finding | 129 | 21 | 0.100 | None | 0 | |||||||||
|
disease | Infections; Respiratory Tract Diseases | Finding | 62 | 11 | 0.100 | None | 0 | ||||||||
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disease | Pathological Conditions, Signs and Symptoms; Musculoskeletal Diseases; Nervous System Diseases | Disease or Syndrome | 50 | 5 | 0.100 | None | 0 | ||||||||
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phenotype | Finding | 11 | 0.100 | None | 0 | ||||||||||
|
phenotype | Finding | 96 | 11 | 0.100 | None | 0 | |||||||||
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disease | Musculoskeletal Diseases | Finding | 210 | 32 | 0.100 | None | 0 | ||||||||
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disease | Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Skin and Connective Tissue Diseases | Disease or Syndrome | 49 | 15 | 0.100 | None | 0 | ||||||||
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phenotype | Stomatognathic Diseases | Finding | 100 | 5 | 0.100 | None | 0 | ||||||||
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phenotype | Nervous System Diseases | Finding | 64 | 2 | 0.100 | None | 0 | ||||||||
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phenotype | Pathological Conditions, Signs and Symptoms; Nervous System Diseases | Finding | 539 | 19 | 0.100 | None | 0 | ||||||||
|
phenotype | Pathological Conditions, Signs and Symptoms; Musculoskeletal Diseases; Nervous System Diseases | Sign or Symptom | 32 | 2 | 0.100 | None | 0 | ||||||||
|
phenotype | Finding | 3 | 0.100 | None | 0 | ||||||||||
|
phenotype | Finding | 45 | 6 | 0.100 | None | 0 | |||||||||
|
phenotype | Finding | 6 | 0.100 | None | 0 | ||||||||||
|
phenotype | Finding | 79 | 8 | 0.100 | None | 0 |