KANSL1, KAT8 regulatory NSL complex subunit 1, 284058
N. diseases: 140; N. variants: 332
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 | Finding | 955 | 164 | 0.100 | None | 0 | ||||||||
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phenotype | Finding | 305 | 22 | 0.100 | None | 0 | |||||||||
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phenotype | Finding | 125 | 8 | 0.100 | None | 0 | 1 | ||||||||
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phenotype | Finding | 96 | 19 | 0.100 | None | 0 | |||||||||
|
disease | Musculoskeletal Diseases | Anatomical Abnormality | 26 | 7 | 0.100 | None | 0 | 1 | |||||||
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phenotype | Finding | 40 | 5 | 0.100 | None | 0 | |||||||||
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phenotype | Finding | 96 | 11 | 0.100 | None | 0 | |||||||||
|
phenotype | Finding | 123 | 13 | 0.100 | None | 0 | |||||||||
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disease | Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases; Nervous System Diseases; Stomatognathic Diseases | Congenital Abnormality | 497 | 70 | 0.100 | None | 0 | ||||||||
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phenotype | Finding | 16 | 8 | 0.100 | None | 0 | |||||||||
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disease | Congenital Abnormality | 188 | 18 | 0.100 | None | 0 | |||||||||
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phenotype | Finding | 137 | 0.100 | None | 0 | ||||||||||
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disease | Eye Diseases; Nervous System Diseases | Disease or Syndrome | 716 | 89 | 0.100 | None | 0 | ||||||||
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phenotype | Finding | 129 | 21 | 0.100 | None | 0 | |||||||||
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disease | Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases | Disease or Syndrome | 187 | 23 | 0.100 | None | 0 | ||||||||
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phenotype | Finding | 182 | 12 | 0.100 | None | 0 | |||||||||
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phenotype | Musculoskeletal Diseases | Pathologic Function | 224 | 15 | 0.100 | None | 0 | ||||||||
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disease | Cardiovascular Diseases | Congenital Abnormality | 154 | 23 | 0.100 | None | 0 | ||||||||
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phenotype | Skin and Connective Tissue Diseases | Sign or Symptom | 159 | 12 | 0.100 | None | 0 | ||||||||
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disease | Musculoskeletal Diseases; Wounds and Injuries | Anatomical Abnormality | 128 | 16 | 0.100 | None | 0 | ||||||||
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phenotype | Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Stomatognathic Diseases | Finding | 140 | 16 | 0.100 | None | 0 | ||||||||
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phenotype | Finding | 20 | 5 | 0.100 | None | 0 | |||||||||
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disease | Cardiovascular Diseases | Disease or Syndrome | 106 | 40 | 0.100 | None | 0 | ||||||||
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phenotype | Behavior and Behavior Mechanisms | Finding | 560 | 192 | 0.100 | None | 0 | ||||||||
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phenotype | Finding | 17 | 0.100 | None | 0 |