TWIST1, twist family bHLH transcription factor 1, 7291
N. diseases: 559; N. variants: 31
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 | 53 | 1 | 0.100 | None | 0 | |||||||||
|
phenotype | Finding | 22 | 10 | 0.100 | None | 0 | |||||||||
|
phenotype | Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases | Finding | 590 | 77 | 0.100 | None | 0 | ||||||||
|
disease | Finding | 9 | 0.100 | None | 0 | ||||||||||
|
phenotype | Finding | 228 | 0.100 | None | 0 | ||||||||||
|
phenotype | Finding | 83 | 7 | 0.100 | None | 0 | |||||||||
|
disease | Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases; Stomatognathic Diseases | Congenital Abnormality | 586 | 53 | 0.100 | None | 0 | ||||||||
|
group | Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Female Urogenital Diseases and Pregnancy Complications; Otorhinolaryngologic Diseases | Congenital Abnormality | 137 | 5 | 0.100 | None | 0 | ||||||||
|
phenotype | Finding | 1127 | 292 | 0.100 | None | 0 | |||||||||
|
phenotype | Finding | 14 | 0.100 | None | 0 | ||||||||||
|
disease | Anatomical Abnormality | 11 | 0.100 | None | 0 | ||||||||||
|
disease | Anatomical Abnormality | 17 | 0.100 | None | 0 | ||||||||||
|
disease | Anatomical Abnormality | 2 | 0.100 | None | 0 | ||||||||||
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phenotype | Finding | 5 | 0.100 | None | 0 | ||||||||||
|
disease | Anatomical Abnormality | 2 | 0.100 | None | 0 | ||||||||||
|
disease | Anatomical Abnormality | 3 | 1 | 0.100 | None | 0 | 1 | ||||||||
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disease | Eye Diseases | Disease or Syndrome | 44 | 6 | 0.100 | None | 0 | ||||||||
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disease | Congenital Abnormality | 154 | 26 | 0.100 | None | 0 | |||||||||
|
disease | Congenital Abnormality | 489 | 64 | 0.100 | None | 0 | |||||||||
|
disease | Anatomical Abnormality | 23 | 0.100 | None | 0 | ||||||||||
|
phenotype | Finding | 211 | 17 | 0.100 | None | 0 | |||||||||
|
disease | Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases; Mental Disorders | Congenital Abnormality | 226 | 26 | 0.100 | None | 0 | ||||||||
|
phenotype | Stomatognathic Diseases | Congenital Abnormality | 38 | 0.100 | None | 0 | |||||||||
|
disease | Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases | Congenital Abnormality | 129 | 11 | 0.100 | None | 0 | ||||||||
|
disease | Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases | Congenital Abnormality | 56 | 15 | 0.100 | None | 0 |