SYNE2, spectrin repeat containing nuclear envelope protein 2, 23224
N. diseases: 91; N. variants: 23
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 | Anatomical Abnormality | 32 | 6 | 0.100 | None | 0 | |||||||||
|
phenotype | Laboratory or Test Result | 11 | 0.100 | None | 0 | ||||||||||
|
phenotype | Finding | 50 | 4 | 0.100 | None | 0 | |||||||||
|
group | Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases; Nervous System Diseases | Disease or Syndrome | 118 | 37 | 0.100 | None | 0 | ||||||||
|
phenotype | Nutritional and Metabolic Diseases | Finding | 23 | 318 | 0.100 | None | 0 | ||||||||
|
phenotype | Pathological Conditions, Signs and Symptoms; Cardiovascular Diseases | Disease or Syndrome | 19 | 2 | 0.100 | None | 0 | ||||||||
|
phenotype | Finding | 7 | 0.100 | None | 0 | ||||||||||
|
phenotype | Finding | 6 | 0.100 | None | 0 | ||||||||||
|
phenotype | Musculoskeletal Diseases; Nervous System Diseases | Pathologic Function | 115 | 16 | 0.100 | None | 0 | ||||||||
|
phenotype | Pathological Conditions, Signs and Symptoms; Nervous System Diseases | Finding | 121 | 8 | 0.100 | None | 0 | ||||||||
|
phenotype | Finding | 9 | 0.100 | None | 0 | ||||||||||
|
phenotype | Finding | 22 | 3 | 0.100 | None | 0 | |||||||||
|
phenotype | Finding | 30 | 4 | 0.100 | None | 0 | |||||||||
|
phenotype | Finding | 55 | 3 | 0.100 | None | 0 | |||||||||
|
phenotype | Finding | 28 | 2 | 0.100 | None | 0 | |||||||||
|
disease | Disease or Syndrome | 29 | 1 | 0.100 | None | 0 | |||||||||
|
phenotype | Finding | 56 | 0.100 | None | 0 | ||||||||||
|
phenotype | Finding | 15 | 4 | 0.100 | None | 0 | |||||||||
|
phenotype | Respiratory Tract Diseases | Finding | 85 | 3 | 0.100 | None | 0 | ||||||||
|
disease | Disease or Syndrome | 16 | 0.100 | None | 0 | ||||||||||
|
phenotype | Finding | 73 | 3 | 0.100 | None | 0 | |||||||||
|
disease | Pathological Conditions, Signs and Symptoms; Respiratory Tract Diseases; Nervous System Diseases; Otorhinolaryngologic Diseases | Disease or Syndrome | 42 | 3 | 0.100 | None | 0 | ||||||||
|
disease | Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases | Congenital Abnormality | 272 | 36 | 0.100 | None | 0 | ||||||||
|
phenotype | Respiratory Tract Diseases | Pathologic Function | 315 | 15 | 0.100 | None | 0 | ||||||||
|
phenotype | Nutritional and Metabolic Diseases | Disease or Syndrome | 340 | 169 | 0.100 | None | 0 |