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| created at |
2021-12-20 02:12:37 UTC |
| updated at |
2021-12-22 07:05:13 UTC |
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MONDO_prefferred_names from the Bioportal site.
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24,286 entries
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There is 0 pattern entry.
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spondylometaphyseal dysplasia, Sedaghatian type
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9593.0 |
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mild hemophilia A
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15721.0 |
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infantile diarrhea
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43555.0 |
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shoulder and girdle defects-familial intellectual disability syndrome
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16821.0 |
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c12orf65-related combined oxidative phosphorylation defect
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44655.0 |
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Axenfeld-Rieger syndrome
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19187.0 |
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congenital narrowing of cervical spinal canal
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19357.0 |
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premature ovarian failure 15
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54862.0 |
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obsolete c3hex, ability to smell
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44281.0 |
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oligodendroglioma
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16695.0 |
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congenital contractures
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22823.0 |
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phacolytic glaucoma
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1553.0 |
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ABri amyloidosis
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8306.0 |
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Kleefstra syndrome due to a point mutation
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16865.0 |
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ameloblastoma
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17795.0 |
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