NOD2, nucleotide binding oligomerization domain containing 2, 64127
N. diseases: 434; N. variants: 107
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 | Pathological Conditions, Signs and Symptoms | Sign or Symptom | 632 | 63 | 0.100 | None | 0 | ||||||||
|
disease | Finding | 2 | 1 | 0.300 | limited | 0 | |||||||||
|
phenotype | Finding | 108 | 0.100 | None | 0 | ||||||||||
|
disease | Digestive System Diseases | Disease or Syndrome | 87 | 3 | 0.100 | None | 0 | ||||||||
|
phenotype | Finding | 137 | 0.100 | None | 0 | ||||||||||
|
disease | Eye Diseases | Disease or Syndrome | 16 | 0.100 | None | 0 | |||||||||
|
phenotype | Pathological Conditions, Signs and Symptoms; Eye Diseases; Nervous System Diseases | Finding | 115 | 6 | 0.100 | None | 0 | ||||||||
|
phenotype | Pathological Conditions, Signs and Symptoms; Eye Diseases; Nervous System Diseases | Sign or Symptom | 227 | 7 | 0.100 | None | 0 | ||||||||
|
phenotype | Pathological Conditions, Signs and Symptoms | Finding | 345 | 19 | 0.100 | None | 0 | ||||||||
|
disease | Anatomical Abnormality | 12 | 1 | 0.100 | None | 0 | |||||||||
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phenotype | Skin and Connective Tissue Diseases | Pathologic Function | 73 | 11 | 0.100 | None | 0 | ||||||||
|
disease | Musculoskeletal Diseases | Disease or Syndrome | 197 | 0.100 | None | 0 | |||||||||
|
phenotype | Finding | 75 | 8 | 0.100 | None | 0 | |||||||||
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disease | Musculoskeletal Diseases; Wounds and Injuries | Disease or Syndrome | 18 | 0.100 | None | 0 | |||||||||
|
phenotype | Skin and Connective Tissue Diseases | Sign or Symptom | 159 | 12 | 0.100 | None | 0 | ||||||||
|
disease | Eye Diseases | Disease or Syndrome | 14 | 0.100 | None | 0 | |||||||||
|
phenotype | Pathological Conditions, Signs and Symptoms; Skin and Connective Tissue Diseases | Disease or Syndrome | 227 | 8 | 0.100 | None | 0 | ||||||||
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disease | Cardiovascular Diseases | Disease or Syndrome | 21 | 0.100 | None | 0 | |||||||||
|
disease | Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Eye Diseases | Disease or Syndrome | 7 | 3 | 0.100 | None | 0 | ||||||||
|
phenotype | Pathological Conditions, Signs and Symptoms | Finding | 33 | 0.100 | None | 0 | |||||||||
|
disease | Eye Diseases | Disease or Syndrome | 24 | 5 | 0.100 | None | 0 | ||||||||
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disease | Hemic and Lymphatic Diseases | Disease or Syndrome | 847 | 94 | 0.100 | None | 0 | ||||||||
|
disease | Stomatognathic Diseases | Finding | 56 | 1 | 0.100 | None | 0 | ||||||||
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phenotype | Sign or Symptom | 48 | 4 | 0.100 | None | 0 | |||||||||
|
phenotype | Pathological Conditions, Signs and Symptoms | Finding | 76 | 131 | 0.100 | None | 0 |