LARP7, La ribonucleoprotein 7, transcriptional regulator, 51574
N. diseases: 57; N. variants: 10
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. | ||||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
disease | Mental Disorders | Mental or Behavioral Dysfunction | 8 | 5 | 0.100 | None | 0 | ||||||||
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phenotype | Finding | 426 | 39 | 0.100 | None | 0 | |||||||||
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phenotype | Finding | 111 | 16 | 0.100 | None | 0 | |||||||||
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phenotype | Finding | 35 | 5 | 0.100 | None | 0 | |||||||||
|
phenotype | Pathological Conditions, Signs and Symptoms | Finding | 271 | 3 | 0.100 | None | 0 | ||||||||
|
phenotype | Finding | 31 | 6 | 0.100 | None | 0 | |||||||||
|
phenotype | Finding | 87 | 1 | 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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phenotype | Finding | 91 | 16 | 0.100 | None | 0 | |||||||||
|
phenotype | Finding | 95 | 15 | 0.100 | None | 0 | |||||||||
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phenotype | Finding | 12 | 5 | 0.100 | None | 0 | |||||||||
|
phenotype | Finding | 159 | 25 | 0.100 | None | 0 | |||||||||
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phenotype | Mental or Behavioral Dysfunction | 8 | 0.100 | None | 0 | ||||||||||
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phenotype | Anatomical Abnormality | 104 | 131 | 0.100 | None | 0 | 1 | ||||||||
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phenotype | Finding | 182 | 25 | 0.100 | None | 0 | |||||||||
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phenotype | Finding | 121 | 11 | 0.100 | None | 0 | |||||||||
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disease | Anatomical Abnormality | 190 | 12 | 0.100 | None | 0 | |||||||||
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phenotype | Finding | 429 | 29 | 0.100 | None | 0 | |||||||||
|
phenotype | Finding | 71 | 10 | 0.100 | None | 0 | |||||||||
|
phenotype | Finding | 211 | 411 | 0.100 | None | 0 | 1 | ||||||||
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disease | Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Neoplasms; Skin and Connective Tissue Diseases; Cardiovascular Diseases; Wounds and Injuries | Disease or Syndrome | 80 | 9 | 0.100 | None | 0 | ||||||||
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phenotype | Finding | 40 | 1 | 0.100 | None | 0 | |||||||||
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group | Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Cardiovascular Diseases | Congenital Abnormality | 384 | 96 | 0.100 | None | 0 | ||||||||
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disease | Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Stomatognathic Diseases | Congenital Abnormality | 148 | 11 | 0.100 | None | 0 | ||||||||
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phenotype | Finding | 34 | 3 | 0.100 | None | 0 |