AP1S2, adaptor related protein complex 1 subunit sigma 2, 8905
N. diseases: 93; 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 | 477 | 0.100 | None | 0 | ||||||||||
|
phenotype | Finding | 182 | 12 | 0.100 | None | 0 | |||||||||
|
phenotype | Finding | 111 | 16 | 0.100 | None | 0 | |||||||||
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phenotype | Nervous System Diseases | Finding | 410 | 0.100 | None | 0 | |||||||||
|
phenotype | Pathological Conditions, Signs and Symptoms; Nervous System Diseases; Otorhinolaryngologic Diseases | Disease or Syndrome | 740 | 337 | 0.100 | None | 0 | ||||||||
|
disease | Behavior and Behavior Mechanisms | Mental or Behavioral Dysfunction | 261 | 78 | 0.100 | None | 0 | ||||||||
|
phenotype | Pathological Conditions, Signs and Symptoms; Nervous System Diseases | Sign or Symptom | 172 | 17 | 0.100 | None | 0 | ||||||||
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group | Pathological Conditions, Signs and Symptoms; Nervous System Diseases | Finding | 312 | 23 | 0.100 | None | 0 | ||||||||
|
phenotype | Pathologic Function | 306 | 12 | 0.100 | None | 0 | |||||||||
|
phenotype | Finding | 70 | 7 | 0.100 | None | 0 | |||||||||
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phenotype | Pathological Conditions, Signs and Symptoms; Eye Diseases; Nervous System Diseases | Finding | 171 | 54 | 0.100 | None | 0 | ||||||||
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disease | Stomatognathic Diseases | Congenital Abnormality | 181 | 19 | 0.100 | None | 0 | ||||||||
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phenotype | Finding | 1127 | 292 | 0.100 | None | 0 | |||||||||
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disease | Musculoskeletal Diseases | Finding | 210 | 32 | 0.100 | None | 0 | ||||||||
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phenotype | Nutritional and Metabolic Diseases; Nervous System Diseases | Finding | 103 | 8 | 0.100 | None | 0 | ||||||||
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disease | Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases; Nervous System Diseases; Stomatognathic Diseases | Congenital Abnormality | 497 | 70 | 0.100 | None | 0 | ||||||||
|
phenotype | Finding | 96 | 11 | 0.100 | None | 0 | |||||||||
|
phenotype | Finding | 211 | 17 | 0.100 | None | 0 | |||||||||
|
phenotype | Finding | 95 | 15 | 0.100 | None | 0 | |||||||||
|
phenotype | Finding | 159 | 25 | 0.100 | None | 0 | |||||||||
|
phenotype | Finding | 299 | 0.100 | None | 0 | ||||||||||
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disease | Disease or Syndrome | 271 | 13 | 0.100 | None | 0 | |||||||||
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phenotype | Anatomical Abnormality | 17 | 3 | 0.100 | None | 0 | |||||||||
|
phenotype | Finding | 33 | 3 | 0.100 | None | 0 | |||||||||
|
phenotype | Finding | 116 | 5 | 0.100 | None | 0 |