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Genes and associated diseases
Disease |
Gene Symbol |
References |
17,20-Lyase Deficiency |
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11549685, 1515452, 25650406, 19793597, 1740503, 11836339, 2808364, 12466376, 8345056, 8550762, 8027220, 24498484, 24140098, 14671162, 10720067, 8245018, 1714904, 8396144, 9326943 |
21-Hydroxylase Deficiency |
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18381579, 1937474, 24671123, 23891399, 8081391, 1496017, 1406699, 1644925, 2788081, 20661889, 17119906, 12915679, 18445671, 24077358, 8968761, 3267225, 19750867, 7635470, 21098686, 9215318, 25227725, 14715874, 9661649, 1864962, 10496074, 23142378, 22270556, 16427797, 8175971, 2466741 |
22q13.3 Deletion Syndrome |
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3 beta-Hydroxysteroid dehydrogenase deficiency |
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7608265, 22579964, 7833923, 7633426, 8126127, 12050213, 10843183, 8060486, 7962268, 8185809, 7633460, 9719627, 10651755, 7893703, 18252794, 8316254, 295036, 8284113, 10770215, 1363812, 10599696, 24033266, 25526675 |
5-Alpha Reductase Deficiency |
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Acquired Language Disorders |
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Activated Protein C Resistance |
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Acute Coronary Syndrome |
ACTG1, APOE, CRP, GSTP1, IL6, LPA, MMP9, PLA2G7, PON1, SERPINC1, SOD2, TNF, VIM, CD14, FASN, S100A12, IGFBP4, ANGPTL2, LAP, MIR223 |
21751358, 28753643, 23305094, 15966572, 20981132, 26241956, 7923645, 24583418, 22490687, 28157385, 29526675, 26025773, 27101308, 25612606, 26646931, 28734158, 24202700 |
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