SMARCA2, SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily a, member 2, 6595
N. diseases: 189; N. variants: 41
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 | 133 | 13 | 0.100 | None | 0 | 1 | ||||||||
|
disease | Pathological Conditions, Signs and Symptoms; Nervous System Diseases | Disease or Syndrome | 533 | 12 | 0.100 | None | 0 | ||||||||
|
disease | Pathological Conditions, Signs and Symptoms; Nervous System Diseases; Mental Disorders; Behavior and Behavior Mechanisms | Mental or Behavioral Dysfunction | 429 | 74 | 0.100 | None | 0 | ||||||||
|
phenotype | Finding | 71 | 10 | 0.100 | None | 0 | |||||||||
|
disease | Endocrine System Diseases | Disease or Syndrome | 139 | 20 | 0.100 | None | 0 | 1 | |||||||
|
phenotype | Finding | 112 | 9 | 0.100 | None | 0 | 1 | ||||||||
|
phenotype | Finding | 1127 | 292 | 0.100 | None | 0 | |||||||||
|
phenotype | Finding | 91 | 16 | 0.100 | None | 0 | |||||||||
|
phenotype | Finding | 391 | 49 | 0.100 | None | 0 | |||||||||
|
disease | Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Skin and Connective Tissue Diseases | Congenital Abnormality | 19 | 1 | 0.100 | None | 0 | ||||||||
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phenotype | Finding | 295 | 14 | 0.100 | None | 0 | |||||||||
|
phenotype | Finding | 64 | 4 | 0.100 | None | 0 | |||||||||
|
disease | Mental or Behavioral Dysfunction | 1825 | 553 | 0.100 | None | 0 | 1 | ||||||||
|
phenotype | Finding | 99 | 8 | 0.100 | None | 0 | |||||||||
|
phenotype | Finding | 66 | 7 | 0.100 | None | 0 | |||||||||
|
phenotype | Finding | 41 | 1 | 0.100 | None | 0 | |||||||||
|
disease | Pathological Conditions, Signs and Symptoms; Nervous System Diseases | Disease or Syndrome | 63 | 4 | 0.100 | None | 0 | ||||||||
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phenotype | Finding | 105 | 10 | 0.100 | None | 0 | |||||||||
|
disease | Nervous System Diseases | Disease or Syndrome | 75 | 9 | 0.100 | None | 0 | ||||||||
|
phenotype | Finding | 96 | 19 | 0.100 | None | 0 | |||||||||
|
phenotype | Finding | 111 | 16 | 0.100 | None | 0 | |||||||||
|
phenotype | Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Stomatognathic Diseases | Finding | 140 | 16 | 0.100 | None | 0 | 1 | |||||||
|
phenotype | Finding | 129 | 21 | 0.100 | None | 0 | |||||||||
|
disease | Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases | Congenital Abnormality | 325 | 43 | 0.100 | None | 0 | ||||||||
|
phenotype | Finding | 271 | 106 | 0.100 | None | 0 | 1 |