DNAJC21, DnaJ heat shock protein family (Hsp40) member C21, 134218
N. diseases: 101; N. variants: 7
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 | Disease or Syndrome | 1 | 6 | 0.600 | strong | 1.000 | 2 | 6 | 2016 | 2018 | |||||
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phenotype | Finding | 3 | 0.100 | None | 0 | ||||||||||
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disease | Disease or Syndrome | 4 | 2 | 0.300 | None | 0 | |||||||||
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disease | Disease or Syndrome | 4 | 2 | 0.300 | None | 0 | |||||||||
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phenotype | Finding | 7 | 0.100 | None | 0 | ||||||||||
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phenotype | Finding | 7 | 0.100 | None | 0 | ||||||||||
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phenotype | Finding | 7 | 0.100 | None | 0 | ||||||||||
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phenotype | Finding | 8 | 0.100 | None | 0 | ||||||||||
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phenotype | Finding | 9 | 0.100 | None | 0 | ||||||||||
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phenotype | Finding | 10 | 0.100 | None | 0 | ||||||||||
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disease | Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Neoplasms; Hemic and Lymphatic Diseases | Disease or Syndrome | 11 | 3 | 0.100 | None | 1.000 | 1 | 3 | 2016 | 2016 | ||||
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disease | Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Eye Diseases; Skin and Connective Tissue Diseases; Nervous System Diseases; Mental Disorders; Behavior and Behavior Mechanisms | Disease or Syndrome | 14 | 3 | 0.010 | None | 1.000 | 1 | 2008 | 2008 | |||||
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disease | Musculoskeletal Diseases | Disease or Syndrome | 15 | 0.100 | None | 0 | |||||||||
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disease | Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases | Congenital Abnormality | 20 | 3 | 0.100 | None | 0 | ||||||||
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phenotype | Finding | 25 | 2 | 0.100 | None | 0 | 1 | ||||||||
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phenotype | Finding | 25 | 0.100 | None | 0 | ||||||||||
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disease | Cardiovascular Diseases | Disease or Syndrome | 30 | 2 | 0.100 | None | 0 | ||||||||
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phenotype | Digestive System Diseases; Nutritional and Metabolic Diseases | Finding | 37 | 0.100 | None | 0 | |||||||||
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disease | Disease or Syndrome | 41 | 0.300 | None | 0 | ||||||||||
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phenotype | Finding | 43 | 3 | 0.100 | None | 0 | |||||||||
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phenotype | Congenital Abnormality | 45 | 7 | 0.100 | None | 0 | |||||||||
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disease | Disease or Syndrome | 49 | 13 | 0.520 | None | 1.000 | 3 | 2017 | 2019 | ||||||
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phenotype | Pathological Conditions, Signs and Symptoms; Musculoskeletal Diseases | Finding | 49 | 2 | 0.100 | None | 0 | ||||||||
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phenotype | Finding | 51 | 8 | 0.100 | None | 0 | |||||||||
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phenotype | Finding | 52 | 0.100 | None | 0 |