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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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haemopericardium
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5783 |
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hemopericardium
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5783 |
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irideremia
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D015783 |
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hemopericardium (disease)
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5783 |
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whyte syndrome
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C535783 |
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whyte petersen McAlister syndrome
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C535783 |
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Prader-Willi syndrome due to paternal deletion of 15q11q13 type 1
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15783 |
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chromosome 15q11-q13 duplication syndrome
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C557830 |
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microdeletion 15q11.2
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C557830 |
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duplication 15q11-q13 syndrome
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C557830 |
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absent iris
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D015783 |
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congenital aniridia
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D015783 |
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Lemierre's disease
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D057831 |
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disease, Lemierre's
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D057831 |
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disease, lemierre
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D057831 |
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