NDUFAF3, NADH:ubiquinone oxidoreductase complex assembly factor 3, 25915
N. diseases: 101; N. variants: 4
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 | 11 | 1 | 0.100 | None | 0 | |||||||||
|
phenotype | Finding | 146 | 7 | 0.100 | None | 0 | |||||||||
|
disease | Anatomical Abnormality | 10 | 0.100 | None | 0 | ||||||||||
|
disease | Anatomical Abnormality | 39 | 2 | 0.100 | None | 0 | |||||||||
|
phenotype | Finding | 33 | 2 | 0.100 | None | 0 | |||||||||
|
phenotype | Finding | 7 | 2 | 0.100 | None | 0 | |||||||||
|
disease | Pathological Conditions, Signs and Symptoms | Anatomical Abnormality | 34 | 4 | 0.100 | None | 0 | ||||||||
|
disease | Anatomical Abnormality | 10 | 0.100 | None | 0 | ||||||||||
|
phenotype | Anatomical Abnormality | 9 | 1 | 0.100 | None | 0 | |||||||||
|
phenotype | Finding | 477 | 0.100 | None | 0 | ||||||||||
|
phenotype | Finding | 779 | 0.100 | None | 0 | ||||||||||
|
group | Nervous System Diseases | Disease or Syndrome | 549 | 69 | 0.100 | None | 0 | ||||||||
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phenotype | Pathological Conditions, Signs and Symptoms; Respiratory Tract Diseases | Finding | 16 | 1 | 0.100 | None | 0 | ||||||||
|
group | Pathological Conditions, Signs and Symptoms; Nervous System Diseases; Mental Disorders; Behavior and Behavior Mechanisms | Mental or Behavioral Dysfunction | 2165 | 159 | 0.100 | None | 0 | ||||||||
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phenotype | Eye Diseases | Finding | 50 | 14 | 0.100 | None | 0 | ||||||||
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disease | Cardiovascular Diseases | Disease or Syndrome | 106 | 40 | 0.100 | None | 0 | ||||||||
|
phenotype | Finding | 108 | 0.100 | None | 0 | ||||||||||
|
phenotype | Finding | 779 | 0.100 | None | 0 | ||||||||||
|
phenotype | Finding | 41 | 3 | 0.100 | None | 0 | |||||||||
|
phenotype | Finding | 8 | 0.100 | None | 0 | ||||||||||
|
phenotype | Pathological Conditions, Signs and Symptoms | Finding | 10 | 0.100 | None | 0 | |||||||||
|
phenotype | Finding | 427 | 32 | 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 | 95 | 3 | 0.100 | None | 0 | ||||||||
|
phenotype | Pathological Conditions, Signs and Symptoms; Eye Diseases; Nervous System Diseases | Finding | 422 | 0.100 | None | 0 | |||||||||
|
phenotype | Pathological Conditions, Signs and Symptoms; Nervous System Diseases | Finding | 118 | 24 | 0.100 | None | 0 |