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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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neoplasms, lip
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D008048 |
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heparin-induced thrombocytopenia (disease)
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18048 |
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centronuclear myopathy, autosomal dominant
|
8048 |
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myopathy, centronuclear, autosomal dominant
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8048 |
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myotubular myopathy, autosomal dominant
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8048 |
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autosomal dominant centronuclear myopathy
|
8048 |
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DNM2-related centronuclear myopathy
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8048 |
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sudden unexpected death in epilepsy
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D000080485 |
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trisomy 17p chromosome 17
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C538048 |
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heparin-induced thrombocytopenia type 2
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18048 |
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chromosome 17, trisomy 17p
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C538048 |
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cancer of the lip
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D008048 |
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myopathy, centronuclear, type 1
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8048 |
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