ADAMTS2, ADAM metallopeptidase with thrombospondin type 1 motif 2, 9509
N. diseases: 138; N. variants: 13
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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disease | Congenital Abnormality | 417 | 30 | 0.100 | None | 0 | |||||||||
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phenotype | Musculoskeletal Diseases | Sign or Symptom | 163 | 14 | 0.100 | None | 0 | ||||||||
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phenotype | Finding | 39 | 3 | 0.100 | None | 0 | |||||||||
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phenotype | Female Urogenital Diseases and Pregnancy Complications | Pathologic Function | 192 | 50 | 0.100 | None | 0 | ||||||||
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phenotype | Musculoskeletal Diseases | Pathologic Function | 224 | 15 | 0.100 | None | 0 | ||||||||
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phenotype | Finding | 95 | 15 | 0.100 | None | 0 | |||||||||
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phenotype | Finding | 11 | 4 | 0.100 | None | 0 | |||||||||
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phenotype | Finding | 105 | 3 | 0.100 | None | 0 | |||||||||
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phenotype | Mental Disorders | Finding | 384 | 34 | 0.100 | None | 0 | ||||||||
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phenotype | Finding | 1 | 0.100 | None | 0 | ||||||||||
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disease | Musculoskeletal Diseases | Disease or Syndrome | 850 | 135 | 0.100 | None | 0 | ||||||||
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phenotype | Finding | 26 | 5 | 0.100 | None | 0 | |||||||||
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disease | Nutritional and Metabolic Diseases; Musculoskeletal Diseases | Disease or Syndrome | 72 | 16 | 0.100 | None | 0 | ||||||||
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phenotype | Stomatognathic Diseases | Finding | 1 | 0.100 | None | 0 | |||||||||
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disease | Disease or Syndrome | 1 | 0.100 | None | 0 | ||||||||||
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disease | Nutritional and Metabolic Diseases; Musculoskeletal Diseases | Disease or Syndrome | 1098 | 182 | 0.100 | None | 0 | ||||||||
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disease | Nutritional and Metabolic Diseases; Musculoskeletal Diseases | Disease or Syndrome | 845 | 61 | 0.100 | None | 0 | ||||||||
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phenotype | Finding | 71 | 5 | 0.100 | None | 0 | |||||||||
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phenotype | Finding | 426 | 39 | 0.100 | None | 0 | |||||||||
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phenotype | Finding | 56 | 3 | 0.100 | None | 0 | |||||||||
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phenotype | Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Skin and Connective Tissue Diseases | Pathologic Function | 48 | 2 | 0.100 | None | 0 | ||||||||
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phenotype | Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Eye Diseases | Finding | 70 | 13 | 0.100 | None | 0 | ||||||||
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disease | Pathological Conditions, Signs and Symptoms; Nervous System Diseases; Mental Disorders; Behavior and Behavior Mechanisms | Disease or Syndrome | 393 | 2 | 0.100 | None | 0 | ||||||||
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disease | Pathological Conditions, Signs and Symptoms; Nervous System Diseases | Disease or Syndrome | 63 | 4 | 0.100 | None | 0 | ||||||||
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phenotype | Wounds and Injuries | Finding | 133 | 14 | 0.100 | None | 0 |