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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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fluid leakage, cerebrospinal
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43327 |
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csf - cerebrospinal fluid leak
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43327 |
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childhood-onset benign chorea with striatal involvement
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44332 |
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obsolete ovarian choriocarcinoma
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6332.0 |
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glycoprotein IIb/IIIa defect
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31332 |
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rare developmental defect with connective tissue involvement
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15332.0 |
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short stature-delayed bone age due to thyroid hormone metabolism deficiency
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12332 |
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primary hyperoxaluria caused by mutation in HOGA1
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13327 |
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Senior-Loken syndrome caused by mutation in SDCCAG8
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13326 |
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cranioectodermal dysplasia caused by mutation in WDR35
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13323 |
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retinitis pigmentosa caused by mutation in ZNF513
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13328 |
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Neorickettsia sennetsu caused disease or disorder
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332 |
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chromosome 16p12.2-p11.2 deletion syndrome, 7.1- to 8.7-MB
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13320 |
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noninsulin-dependent, 2 diabetes mellitus
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C563323 |
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pseudo-VON WILLEBRAND disease
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8332 |
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