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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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progressive bifocal chorioretinal atrophy
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10932.0 |
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syndromic X-linked intellectual disability Hedera type
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10319.0 |
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hereditary spastic paraplegia 24
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11862.0 |
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keratoderma hereditarium mutilans
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7422.0 |
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hemicrania continua
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18615.0 |
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global developmental delay - lung cysts - overgrowth - Wilms tumor syndrome
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18445.0 |
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neurofibroma of gallbladder
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3303.0 |
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type 1 papillary adenoma of the kidney
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3830.0 |
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camera-Marugo-Cohen syndrome
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11419.0 |
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hereditary arterial and articular multiple calcification syndrome
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8895.0 |
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high grade astrocytic tumor
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16680.0 |
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behrens baumann dust syndrome
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22557.0 |
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familial hemophagocytic lymphohistiocytosis 3
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12146.0 |
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urinary bladder small cell neuroendocrine carcinoma
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4114.0 |
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periodic fever syndrome
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15137.0 |
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