MAP3K7, mitogen-activated protein kinase kinase kinase 7, 6885
N. diseases: 273; 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. | ||||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
disease | Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases | Disease or Syndrome | 253 | 18 | 0.100 | None | 0 | ||||||||
|
phenotype | Finding | 116 | 0.100 | None | 0 | ||||||||||
|
phenotype | Finding | 64 | 4 | 0.100 | None | 0 | |||||||||
|
phenotype | Finding | 295 | 14 | 0.100 | None | 0 | |||||||||
|
disease | Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases | Anatomical Abnormality | 10 | 0.100 | None | 0 | |||||||||
|
disease | Congenital Abnormality | 15 | 0.100 | None | 0 | ||||||||||
|
disease | Congenital Abnormality | 176 | 23 | 0.100 | None | 0 | |||||||||
|
phenotype | Finding | 125 | 8 | 0.100 | None | 0 | |||||||||
|
phenotype | Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases | Finding | 134 | 14 | 0.100 | None | 0 | ||||||||
|
phenotype | Finding | 391 | 49 | 0.100 | None | 0 | |||||||||
|
phenotype | Finding | 216 | 16 | 0.100 | None | 0 | |||||||||
|
disease | Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases | Congenital Abnormality | 123 | 10 | 0.100 | None | 0 | ||||||||
|
disease | Cardiovascular Diseases | Disease or Syndrome | 111 | 29 | 0.100 | None | 0 | ||||||||
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phenotype | Cardiovascular Diseases | Pathologic Function | 94 | 11 | 0.100 | None | 0 | ||||||||
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phenotype | Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases | Finding | 590 | 77 | 0.100 | None | 0 | ||||||||
|
phenotype | Finding | 407 | 35 | 0.100 | None | 0 | |||||||||
|
phenotype | Finding | 42 | 5 | 0.100 | None | 0 | |||||||||
|
phenotype | Finding | 89 | 0.100 | None | 0 | ||||||||||
|
phenotype | Finding | 129 | 21 | 0.100 | None | 0 | |||||||||
|
phenotype | Finding | 66 | 7 | 0.100 | None | 0 | |||||||||
|
phenotype | Finding | 426 | 39 | 0.100 | None | 0 | |||||||||
|
phenotype | Finding | 23 | 0.100 | None | 0 | ||||||||||
|
disease | Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Cardiovascular Diseases | Anatomical Abnormality | 55 | 14 | 0.100 | None | 0 | ||||||||
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disease | Otorhinolaryngologic Diseases | Disease or Syndrome | 120 | 11 | 0.100 | None | 0 | ||||||||
|
phenotype | Finding | 168 | 7 | 0.100 | None | 0 |