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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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primary, 11 ciliary dyskinesia
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C567212 |
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primary, 10 ciliary dyskinesia
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C567287 |
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neutropenia, severe congenital, autosomal recessive 4
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C567260 |
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lipodystrophy, berardinelli-seip congenital, type 3
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C567282 |
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myopathy, congenital, compton-north
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C567261 |
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adenylate kinase deficiency, hemolytic anemia due to
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C567228 |
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autosomal dominant craniodiaphyseal dysplasia
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C567275 |
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chromosome 15q26-Qter deletion syndrome
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C567232 |
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chromosome 6pter-P24 deletion syndrome
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C567239 |
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chromosome 2p16.1-P15 deletion syndrome
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C567289 |
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chromosome 11p13-P12 deletion syndrome
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C567292 |
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chromosome 1q21.1 deletion syndrome, 1.35-mb
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C567291 |
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Blastomyces dermatitidis disease or disorder
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5672 |
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insulin-dependent, 23 diabetes mellitus
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C567233 |
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insulin-dependent, 22 diabetes mellitus
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C567284 |
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