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| created at |
2021-12-22 03:08:20 UTC |
| updated at |
2021-12-22 07:06:09 UTC |
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MONDO_bioport_pref_name
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183,974 entries
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There is 0 pattern entry.
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Del(7)(q31)
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16656 |
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aortitis
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6656 |
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monosomy 7q31
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16656 |
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aorta inflammation
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6656 |
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peroxisome biogenesis disorder, complementation group e
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C566569 |
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complementation group 1 peroxisome biogenesis disorder
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C566568 |
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inflammation of aorta
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6656 |
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medium chain 3-Ketoacyl-CoA thiolase deficiency
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C566566 |
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7q31 microdeletion syndrome
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16656 |
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retinal pigment epithelium lesions, discolored teeth sensorineural hearing loss
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C566560 |
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complementation group e peroxisome biogenesis disorder
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C566569 |
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