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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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FASTKD2-related infantile mitochondrial encephalomyopathy
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15632.0 |
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verbal auditory agnosia
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684.0 |
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coloboma of iris (disease)
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20356.0 |
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acute megakaryoblastic leukemia in down syndrome
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20526.0 |
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benign neoplasm of sternum
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21456.0 |
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autoimmune encephalopathy with parasomnia and obstructive sleep apnea
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18489.0 |
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oculo-cerebral dysplasia
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22556.0 |
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primary interstitial lung disease specific to childhood due to alveolar structure disorder
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17016.0 |
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syndromic genetic deafness
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19589.0 |
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3p- syndrome
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13424.0 |
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microcephaly, seizures, and developmental delay
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13254.0 |
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obsolete dentin dysplasia
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4073.0 |
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immunodeficiency 62
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32763.0 |
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renal cysts and diabetes syndrome
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7669.0 |
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obsolete pigmented villonodular synovitis
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19021.0 |
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