CPLANE1, ciliogenesis and planar polarity effector 1, 65250
N. diseases: 120; N. variants: 86
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. | ||||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
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disease | Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases | Congenital Abnormality | 180 | 101 | 0.100 | None | 0 | ||||||||
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phenotype | Finding | 8 | 0.100 | None | 0 | ||||||||||
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disease | Congenital Abnormality | 417 | 30 | 0.100 | None | 0 | |||||||||
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phenotype | Finding | 180 | 8 | 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 | Finding | 60 | 0.100 | None | 0 | ||||||||||
|
phenotype | Finding | 9 | 0.100 | None | 0 | ||||||||||
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disease | Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases | Congenital Abnormality | 49 | 0.100 | None | 0 | |||||||||
|
disease | Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases | Anatomical Abnormality | 9 | 0.100 | None | 0 | |||||||||
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phenotype | Finding | 42 | 0.100 | None | 0 | ||||||||||
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phenotype | Finding | 407 | 35 | 0.100 | None | 0 | |||||||||
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phenotype | Finding | 182 | 12 | 0.100 | None | 0 | |||||||||
|
phenotype | Finding | 89 | 0.100 | None | 0 | ||||||||||
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disease | Neoplasms; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases | Disease or Syndrome | 81 | 3 | 0.100 | None | 0 | ||||||||
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phenotype | Finding | 100 | 26 | 0.100 | None | 0 | |||||||||
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disease | Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases | Disease or Syndrome | 110 | 0.100 | None | 0 | |||||||||
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phenotype | Nervous System Diseases | Finding | 15 | 0.100 | None | 0 | |||||||||
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phenotype | Finding | 9 | 0.100 | None | 0 | ||||||||||
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phenotype | Finding | 223 | 19 | 0.100 | None | 0 | |||||||||
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disease | Pathological Conditions, Signs and Symptoms; Eye Diseases; Nervous System Diseases; Behavior and Behavior Mechanisms; Cardiovascular Diseases | Disease or Syndrome | 92 | 14 | 0.100 | None | 0 | ||||||||
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disease | Disease or Syndrome | 8 | 1 | 0.100 | None | 0 | |||||||||
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disease | Anatomical Abnormality | 6 | 2 | 0.100 | None | 0 | |||||||||
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disease | Pathologic Function | 34 | 3 | 0.100 | None | 0 | |||||||||
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disease | Congenital Abnormality | 85 | 28 | 0.100 | None | 0 | |||||||||
|
disease | Anatomical Abnormality | 12 | 0.100 | None | 0 |