MAP2K1, mitogen-activated protein kinase kinase 1, 5604
N. diseases: 389; N. variants: 43
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 | 211 | 17 | 0.100 | None | 0 | |||||||||
|
phenotype | Pathologic Function | 19 | 7 | 0.100 | None | 0 | |||||||||
|
disease | Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases | Congenital Abnormality | 325 | 43 | 0.100 | None | 0 | ||||||||
|
phenotype | Finding | 97 | 12 | 0.100 | None | 0 | |||||||||
|
phenotype | Finding | 103 | 4 | 0.100 | None | 0 | |||||||||
|
phenotype | Finding | 60 | 0.100 | None | 0 | ||||||||||
|
disease | Stomatognathic Diseases | Anatomical Abnormality | 128 | 10 | 0.100 | None | 0 | ||||||||
|
disease | Neoplasms | Neoplastic Process | 43 | 1 | 0.100 | None | 0 | ||||||||
|
disease | Eye Diseases; Nervous System Diseases | Disease or Syndrome | 568 | 51 | 0.100 | None | 0 | ||||||||
|
phenotype | Finding | 426 | 39 | 0.100 | None | 0 | |||||||||
|
disease | Digestive System Diseases; Neoplasms | Neoplastic Process | 543 | 432 | 0.300 | None | 0 | ||||||||
|
phenotype | Finding | 42 | 0.100 | None | 0 | ||||||||||
|
phenotype | Finding | 182 | 12 | 0.100 | None | 0 | |||||||||
|
disease | Neoplasms; Female Urogenital Diseases and Pregnancy Complications; Endocrine System Diseases | Neoplastic Process | 539 | 19 | 0.300 | None | 0 | ||||||||
|
disease | Pathological Conditions, Signs and Symptoms | Disease or Syndrome | 607 | 12 | 0.100 | None | 0 | ||||||||
|
phenotype | Finding | 111 | 16 | 0.100 | None | 0 | |||||||||
|
phenotype | Finding | 12 | 2 | 0.100 | None | 0 | |||||||||
|
phenotype | Finding | 35 | 1 | 0.100 | None | 0 | |||||||||
|
disease | Disease or Syndrome | 13 | 12 | 0.100 | None | 0 | |||||||||
|
disease | Musculoskeletal Diseases | Disease or Syndrome | 197 | 0.100 | None | 0 | |||||||||
|
phenotype | Pathological Conditions, Signs and Symptoms; Nervous System Diseases | Sign or Symptom | 2152 | 553 | 0.100 | None | 0 | ||||||||
|
phenotype | Female Urogenital Diseases and Pregnancy Complications | Pathologic Function | 192 | 50 | 0.100 | None | 0 | ||||||||
|
disease | Eye Diseases; Nervous System Diseases | Disease or Syndrome | 833 | 95 | 0.100 | None | 0 | ||||||||
|
phenotype | Nervous System Diseases | Finding | 227 | 27 | 0.100 | None | 0 | ||||||||
|
disease | Acquired Abnormality | 35 | 1 | 0.100 | None | 0 |