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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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fuchs' dystrophy
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C535478 |
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cardiocranial syndrome
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C535578 |
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SCT syndrome
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C535780 |
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synspondylism, congenital
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C535780 |
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whyte syndrome
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C535783 |
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humero-spinal dysostosis
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C535789 |
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humerospinal dysostosis
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C535789 |
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Rud's syndrome
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C535878 |
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11-Beta-hydroxylase deficiency
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C535978 |
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p450c11b1 deficiency
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C535978 |
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anonychia onychodystrophy
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C536378 |
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urioste syndrome
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C536478 |
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snyder-robinson syndrome
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C536678 |
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tabatznik syndrome
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C536784 |
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baller-gerold syndrome
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C536788 |
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