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| language |
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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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intestinal, with secondary hypocalcemia hypomagnesemia
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C566593 |
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obsolete Lennox-Gastaut syndrome
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11665.0 |
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2q31.1 microdeletion syndrome
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16652 |
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2q33.1 microdeletion syndrome
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16653 |
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6p22 microdeletion syndrome
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16655 |
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7q31 microdeletion syndrome
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16656 |
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8p11.2 deletion syndrome
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16657 |
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8p23.1 microdeletion syndrome
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16658 |
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8p23.1 duplication syndrome
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16659 |
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shohat type spondyloepimetaphyseal dysplasia
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C566523 |
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missouri type spondyloepimetaphyseal dysplasia
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C566574 |
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premature aging syndrome, penttinen type
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C536653 |
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congenital, with synergistic divergence fibrosis of extraocular muscles
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C566508 |
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SEMD, shohat type
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C566523 |
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familial broad terminal phalanges
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C566588 |
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