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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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hereditary opalescent dentin
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D003811 |
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ovarian mixed epithelial neoplasm
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3811 |
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ovarian mixed epithelial tumor
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3811 |
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hirschsprung disease ganglioneuroblastoma
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C538119 |
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opalescent dentin, hereditary
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D003811 |
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visceral, X-linked heterotaxy
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C538116 |
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neuroblastoma with hirschsprung disease
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C538119 |
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mixed epithelial neoplasm of ovary
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3811 |
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mixed epithelial neoplasm of the ovary
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3811 |
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congenital absence of insulin-producing beta cells with diabetes mellitus
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C538111 |
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pigmentary abnormality of the anterior segment of the eye
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C538115 |
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dextrocardia with other cardiac malformations
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C538116 |
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MRPL3 combined oxidative phosphorylation deficiency
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13811 |
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combined oxidative phosphorylation defect type 9
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13811 |
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combined oxidative phosphorylation deficiency 9
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13811 |
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