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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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candidiasis, familial chronic mucocutaneous
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13140 |
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communication disorder, childhood
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D003147 |
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communication disorders, childhood
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D003147 |
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CLEC7A familial chronic mucocutaneous candidiasis
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13140 |
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AT III deficiency
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13144 |
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hearing loss, conductive
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D006314 |
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perisylvian syndrome, congenital bilateral
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10314 |
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antithrombin 3 deficiency
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13144 |
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antithrombin III deficiency
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13144 |
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congenital AT-III deficiency
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13144 |
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hereditary antithrombin deficiency
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13144 |
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inherited antithrombin deficiency
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13144 |
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familial isolated dilated cardiomyopathy caused by mutation in NEXN
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13147 |
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calcium pyrophosphate deposition disease
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1314 |
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acquired communication disorder
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D003147 |
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