SURF1, SURF1 cytochrome c oxidase assembly factor, 6834
N. diseases: 150; N. variants: 29
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 | Pathological Conditions, Signs and Symptoms; Nervous System Diseases | Sign or Symptom | 2152 | 553 | 0.110 | None | 1.000 | 1 | 1 | 2014 | 2014 | ||||
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phenotype | Nutritional and Metabolic Diseases | Disease or Syndrome | 209 | 21 | 0.110 | None | 1.000 | 1 | 2013 | 2013 | |||||
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group | Nervous System Diseases | Disease or Syndrome | 549 | 69 | 0.110 | None | 1.000 | 1 | 2000 | 2000 | |||||
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disease | Congenital Abnormality | 439 | 617 | 0.100 | None | 1.000 | 7 | 3 | 1998 | 2016 | |||||
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phenotype | Pathological Conditions, Signs and Symptoms; Nervous System Diseases | Finding | 967 | 579 | 0.100 | None | 1.000 | 7 | 1 | 1998 | 2016 | ||||
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group | Nervous System Diseases | Disease or Syndrome | 362 | 247 | 0.100 | None | 1.000 | 7 | 2 | 1998 | 2016 | ||||
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phenotype | Pathological Conditions, Signs and Symptoms; Nervous System Diseases | Sign or Symptom | 13 | 5 | 0.100 | None | 1.000 | 1 | 1 | 2016 | 2016 | ||||
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phenotype | Finding | 18 | 0.100 | None | 0 | ||||||||||
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phenotype | Finding | 35 | 3 | 0.100 | None | 0 | |||||||||
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disease | Musculoskeletal Diseases | Anatomical Abnormality | 155 | 17 | 0.100 | None | 0 | ||||||||
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disease | Musculoskeletal Diseases | Acquired Abnormality | 149 | 2 | 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 | 20 | 1 | 0.100 | None | 0 | |||||||||
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phenotype | Finding | 103 | 31 | 0.100 | None | 0 | |||||||||
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disease | Mental Disorders | Disease or Syndrome | 333 | 80 | 0.100 | None | 0 | ||||||||
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disease | Respiratory Tract Diseases | Disease or Syndrome | 319 | 23 | 0.100 | None | 0 | ||||||||
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phenotype | Pathological Conditions, Signs and Symptoms; Nervous System Diseases; Otorhinolaryngologic Diseases | Disease or Syndrome | 740 | 337 | 0.100 | None | 0 | ||||||||
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phenotype | Nervous System Diseases | Finding | 410 | 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 | Finding | 16 | 0.100 | None | 0 | ||||||||||
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phenotype | Finding | 87 | 1 | 0.100 | None | 0 | |||||||||
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phenotype | Nervous System Diseases | Pathologic Function | 27 | 3 | 0.100 | None | 0 | ||||||||
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phenotype | Nutritional and Metabolic Diseases | Finding | 169 | 2 | 0.100 | None | 0 | ||||||||
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phenotype | Finding | 74 | 5 | 0.100 | None | 0 | |||||||||
|
phenotype | Finding | 21 | 2 | 0.100 | None | 0 |