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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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syndrome with 46,XX disorder of sex development
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17965.0 |
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Paget disease of the penis
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2653.0 |
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hypertrichotic osteochondrodysplasia Cantu type
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9406.0 |
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hereditary sensory and autonomic neuropathy type 1
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18213.0 |
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dermatosis of eyelid
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24480.0 |
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obsolete blood group, vel system
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44282.0 |
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agenesis of the superior vena cava
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20445.0 |
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indomethacin embryofetopathy
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16005.0 |
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congenital sideroblastic anemia-B-cell immunodeficiency-periodic fever-developmental delay syndrome
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14487.0 |
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obsolete blood group system, landsteiner-wiener
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20615.0 |
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glioependymal/ependymal cyst
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17105.0 |
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developmental and epileptic encephalopathy 89
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30856.0 |
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arteriolosclerosis
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6658.0 |
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nasal cavity and paranasal sinus lethal midline granuloma
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6828.0 |
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juvenile idiopathic inflammatory myopathy
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18010.0 |
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