KCNJ8, potassium inwardly rectifying channel subfamily J member 8, 3764
N. diseases: 84; N. variants: 4
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 | Pathological Conditions, Signs and Symptoms; Skin and Connective Tissue Diseases | Finding | 113 | 3 | 0.100 | None | 0 | ||||||||
|
phenotype | Finding | 288 | 29 | 0.100 | None | 0 | |||||||||
|
phenotype | Cardiovascular Diseases | Finding | 23 | 0.100 | None | 0 | |||||||||
|
phenotype | Finding | 86 | 11 | 0.100 | None | 0 | |||||||||
|
phenotype | Finding | 112 | 18 | 0.100 | None | 0 | |||||||||
|
disease | Congenital, Hereditary, and Neonatal Diseases and Abnormalities | Congenital Abnormality | 186 | 65 | 0.100 | None | 0 | ||||||||
|
phenotype | Finding | 19 | 6 | 0.100 | None | 0 | |||||||||
|
phenotype | Finding | 282 | 16 | 0.100 | None | 0 | |||||||||
|
phenotype | Finding | 23 | 0.100 | None | 0 | ||||||||||
|
phenotype | Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Cardiovascular Diseases | Finding | 42 | 1 | 0.100 | None | 0 | ||||||||
|
phenotype | Pathological Conditions, Signs and Symptoms; Musculoskeletal Diseases | Finding | 68 | 5 | 0.100 | None | 0 | ||||||||
|
phenotype | Finding | 15 | 0.100 | None | 0 | ||||||||||
|
disease | Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases; Nervous System Diseases | Congenital Abnormality | 367 | 10 | 0.100 | None | 0 | ||||||||
|
disease | Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Female Urogenital Diseases and Pregnancy Complications; Musculoskeletal Diseases | Congenital Abnormality | 171 | 12 | 0.100 | None | 0 | ||||||||
|
phenotype | Finding | 295 | 14 | 0.100 | None | 0 | |||||||||
|
phenotype | Finding | 64 | 4 | 0.100 | None | 0 | |||||||||
|
disease | Congenital Abnormality | 417 | 30 | 0.100 | None | 0 | |||||||||
|
phenotype | Finding | 18 | 0.100 | None | 0 | ||||||||||
|
phenotype | Pathological Conditions, Signs and Symptoms | Finding | 194 | 33 | 0.100 | None | 0 | ||||||||
|
phenotype | Finding | 93 | 3 | 0.100 | None | 0 | |||||||||
|
phenotype | Finding | 71 | 17 | 0.100 | None | 0 | |||||||||
|
phenotype | Finding | 41 | 10 | 0.100 | None | 0 | |||||||||
|
phenotype | Finding | 407 | 35 | 0.100 | None | 0 | |||||||||
|
phenotype | Finding | 85 | 3 | 0.100 | None | 0 | |||||||||
|
phenotype | Finding | 95 | 15 | 0.100 | None | 0 |