EIF2S3, eukaryotic translation initiation factor 2 subunit gamma, 1968
N. diseases: 107; N. variants: 6
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; Nervous System Diseases | Sign or Symptom | 172 | 17 | 0.100 | None | 0 | ||||||||
|
disease | Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases | Congenital Abnormality | 385 | 49 | 0.100 | None | 0 | ||||||||
|
disease | Male Urogenital Diseases | Congenital Abnormality | 217 | 11 | 0.100 | None | 0 | ||||||||
|
phenotype | Finding | 211 | 411 | 0.100 | None | 0 | 1 | ||||||||
|
phenotype | Finding | 18 | 2 | 0.100 | None | 0 | |||||||||
|
phenotype | Finding | 71 | 10 | 0.100 | None | 0 | |||||||||
|
phenotype | Finding | 160 | 246 | 0.100 | None | 0 | 1 | ||||||||
|
disease | Anatomical Abnormality | 3 | 2 | 0.100 | None | 0 | |||||||||
|
disease | Disease or Syndrome | 168 | 27 | 0.100 | None | 0 | |||||||||
|
phenotype | Finding | 427 | 32 | 0.100 | None | 0 | |||||||||
|
phenotype | Finding | 779 | 0.100 | None | 0 | ||||||||||
|
phenotype | Finding | 87 | 0.100 | None | 0 | ||||||||||
|
phenotype | Finding | 103 | 4 | 0.100 | None | 0 | |||||||||
|
phenotype | Anatomical Abnormality | 122 | 14 | 0.100 | None | 0 | |||||||||
|
phenotype | Finding | 779 | 0.100 | None | 0 | ||||||||||
|
phenotype | Finding | 282 | 16 | 0.100 | None | 0 | |||||||||
|
phenotype | Finding | 319 | 0.100 | None | 0 | ||||||||||
|
phenotype | Finding | 23 | 3 | 0.100 | None | 0 | |||||||||
|
phenotype | Pathological Conditions, Signs and Symptoms; Nervous System Diseases | Finding | 955 | 164 | 0.100 | None | 0 | ||||||||
|
phenotype | Finding | 149 | 5 | 0.100 | None | 0 | |||||||||
|
phenotype | Finding | 21 | 13 | 0.100 | None | 0 | |||||||||
|
phenotype | Pathological Conditions, Signs and Symptoms; Nervous System Diseases | Finding | 208 | 9 | 0.100 | None | 0 | ||||||||
|
phenotype | Finding | 172 | 1 | 0.100 | None | 0 | |||||||||
|
phenotype | Finding | 87 | 0.100 | None | 0 | ||||||||||
|
disease | Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases; Nervous System Diseases; Endocrine System Diseases | Disease or Syndrome | 154 | 14 | 0.100 | None | 0 |