HECW2, HECT, C2 and WW domain containing E3 ubiquitin protein ligase 2, 57520
N. diseases: 42; N. variants: 8
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 | 779 | 0.100 | None | 0 | ||||||||||
|
disease | Congenital Abnormality | 417 | 30 | 0.100 | None | 0 | |||||||||
|
disease | Behavior and Behavior Mechanisms | Mental or Behavioral Dysfunction | 261 | 78 | 0.100 | None | 0 | ||||||||
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phenotype | Nervous System Diseases | Finding | 410 | 0.100 | None | 0 | |||||||||
|
phenotype | Finding | 31 | 6 | 0.100 | None | 0 | |||||||||
|
phenotype | Finding | 426 | 39 | 0.100 | None | 0 | |||||||||
|
phenotype | Finding | 159 | 25 | 0.100 | None | 0 | |||||||||
|
phenotype | Finding | 129 | 21 | 0.100 | None | 0 | |||||||||
|
phenotype | Finding | 145 | 10 | 0.100 | None | 0 | |||||||||
|
phenotype | Finding | 407 | 35 | 0.100 | None | 0 | |||||||||
|
phenotype | Finding | 228 | 0.100 | None | 0 | ||||||||||
|
phenotype | Finding | 104 | 13 | 0.100 | None | 0 | |||||||||
|
phenotype | Pathological Conditions, Signs and Symptoms; Nervous System Diseases | Finding | 955 | 164 | 0.100 | None | 0 | ||||||||
|
phenotype | Finding | 779 | 0.100 | None | 0 | ||||||||||
|
disease | Mental Disorders | Mental or Behavioral Dysfunction | 4 | 0.100 | None | 0 | |||||||||
|
phenotype | Finding | 271 | 106 | 0.100 | None | 0 | |||||||||
|
phenotype | Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases | Finding | 134 | 14 | 0.100 | None | 0 | ||||||||
|
disease | Eye Diseases; Nervous System Diseases | Disease or Syndrome | 833 | 95 | 0.100 | None | 0 | ||||||||
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disease | Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Stomatognathic Diseases | Congenital Abnormality | 148 | 11 | 0.100 | None | 0 | ||||||||
|
phenotype | Finding | 427 | 32 | 0.100 | None | 0 | |||||||||
|
phenotype | Pathological Conditions, Signs and Symptoms; Nervous System Diseases | Sign or Symptom | 2152 | 553 | 0.100 | None | 0 | ||||||||
|
phenotype | Nervous System Diseases | Finding | 227 | 27 | 0.100 | None | 0 | ||||||||
|
disease | Congenital Abnormality | 188 | 18 | 0.100 | None | 0 | |||||||||
|
disease | Pathological Conditions, Signs and Symptoms; Nervous System Diseases | Disease or Syndrome | 454 | 44 | 0.100 | None | 0 | ||||||||
|
phenotype | Finding | 123 | 13 | 0.100 | None | 0 |