SPECC1L, sperm antigen with calponin homology and coiled-coil domains 1 like, 23384
N. diseases: 117; N. variants: 12
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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phenotype | Finding | 216 | 16 | 0.100 | None | 0 | |||||||||
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disease | Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities | Congenital Abnormality | 235 | 0.100 | None | 0 | |||||||||
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phenotype | Nervous System Diseases | Finding | 410 | 0.100 | None | 0 | |||||||||
|
phenotype | Finding | 56 | 3 | 0.100 | None | 0 | |||||||||
|
phenotype | Finding | 426 | 39 | 0.100 | None | 0 | |||||||||
|
phenotype | Finding | 159 | 25 | 0.100 | None | 0 | |||||||||
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disease | Congenital, Hereditary, and Neonatal Diseases and Abnormalities | Congenital Abnormality | 72 | 4 | 0.100 | None | 0 | ||||||||
|
phenotype | Finding | 100 | 26 | 0.100 | None | 0 | |||||||||
|
phenotype | Finding | 17 | 2 | 0.100 | None | 0 | |||||||||
|
phenotype | Finding | 19 | 0.100 | None | 0 | ||||||||||
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phenotype | Finding | 429 | 29 | 0.100 | None | 0 | |||||||||
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disease | Congenital Abnormality | 284 | 39 | 0.100 | None | 0 | |||||||||
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phenotype | Finding | 105 | 10 | 0.100 | None | 0 | |||||||||
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disease | Behavior and Behavior Mechanisms | Mental or Behavioral Dysfunction | 261 | 78 | 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 | Congenital Abnormality | 366 | 80 | 0.100 | None | 0 | ||||||||
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phenotype | Finding | 391 | 49 | 0.100 | None | 0 | |||||||||
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phenotype | Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases | Finding | 134 | 14 | 0.100 | None | 0 | ||||||||
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phenotype | Finding | 6 | 1 | 0.100 | None | 0 | |||||||||
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disease | Congenital Abnormality | 176 | 23 | 0.100 | None | 0 | |||||||||
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disease | Mental or Behavioral Dysfunction | 1825 | 553 | 0.100 | None | 0 | |||||||||
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phenotype | Finding | 108 | 31 | 0.100 | None | 0 | |||||||||
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phenotype | Finding | 5 | 0.100 | None | 0 | ||||||||||
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phenotype | Finding | 99 | 8 | 0.100 | None | 0 | |||||||||
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disease | Congenital Abnormality | 417 | 30 | 0.100 | None | 0 | |||||||||
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phenotype | Respiratory Tract Diseases | Pathologic Function | 13 | 0.100 | None | 0 |