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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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deafness, autosomal dominant 3b
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C567215 |
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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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Blastomyces dermatitidis disease or disorder
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5672 |
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von willebrand disease, severe form
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D056729 |
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von willebrand disease, type 1
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D056725 |
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von willebrand disease, type 2
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D056728 |
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von willebrand disease, type 2a
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D056728 |
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von willebrand disease, type 2b
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D056728 |
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von willebrand disease, type 2m
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D056728 |
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von willebrand disease, type 2n
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D056728 |
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von willebrand disease, type 3
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D056729 |
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von willebrand disease, type II
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D056728 |
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von willebrand disease, type IIA
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D056728 |
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von willebrand disease, type IIB
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D056728 |
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