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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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limb-girdle, type 2g muscular dystrophy
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C566599 |
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abscess, pyogenic iliopsoas
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D016659 |
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pyogenic iliopsoas abscess
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D016659 |
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thrombocytosis, benign familial microcytic
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C566596 |
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abscesses, pyogenic iliopsoas
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D016659 |
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ectodermal dysplasia, pure hair-nail type
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C566592 |
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muscular dystrophy, limb-girdle, type 2g
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C566599 |
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benign familial microcytic thrombocytosis
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C566596 |
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iliopsoas abscess, pyogenic
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D016659 |
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iliopsoas abscesses, pyogenic
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D016659 |
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intestinal, with secondary hypocalcemia hypomagnesemia
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C566593 |
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myopia, and sensorineural deafness spondyloepiphyseal dysplasia
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C566659 |
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pure hair-nail type ectodermal dysplasia
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C566592 |
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8p23.1 duplication syndrome
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16659 |
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