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| license |
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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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acquired primary erythrocytosis
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9891 |
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polyhydramnios, chronic idiopathic
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9899 |
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KCNT1 early infantile epileptic encephalopathy
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13989 |
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nephrogenic systemic fibroses
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D054989 |
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dermopathies, nephrogenic fibrosing
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D054989 |
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dermopathy, nephrogenic fibrosing
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D054989 |
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Fuchs heterochromic iridocyclitis
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16989 |
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benign fibrous histiocytoma
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2989 |
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benign fibrous histiocytoma (morphologic abnormality)
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2989 |
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diaphragmatic myocardial infarction
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D056989 |
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diaphragmatic myocardial infarctions
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D056989 |
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inferior myocardial infarctions
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D056989 |
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charcot-marie-tooth disease, neuronal, type 2b
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C537989 |
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autosomal dominant, mild xeroderma pigmentosum
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C565989 |
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obsolete non-distal monosomy 7p
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19894.0 |
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