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| created at |
2024-09-23 16:23:50 UTC |
| updated at |
2024-09-23 18:22:39 UTC |
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Terms for rare diseases as defined in ORDO.
The entries were initially sourced from the ORDO version 2024-07-03 as stored in BioPortal.
Namespace: http://www.orpha.net/ORDO/
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20,514 entries
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There is 0 pattern entry.
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Hemophilia A
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Orphanet_98878 |
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Christmas disease
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Orphanet_98879 |
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Hemophilia B
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Orphanet_98879 |
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Familial afibrinogenemia
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Orphanet_98880 |
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Familial dysfibrinogenemia
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Orphanet_98881 |
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Becker dystrophinopathy
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Orphanet_98895 |
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Oculopharyngodistal myopathy
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Orphanet_98897 |
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CDA type 1
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Orphanet_98869 |
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AML with 11q23 abnormalities
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Orphanet_98831 |
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CDA type 2
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Orphanet_98873 |
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CDA type 3
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Orphanet_98870 |
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Primary systemic ALCL
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Orphanet_98841 |
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Intravascular large B-cell lymphoma
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Orphanet_98839 |
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Autosomal recessive Charcot-Marie-Tooth disease type 2B1
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Orphanet_98856 |
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Primary dystonia, DYT13 type
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Orphanet_98807 |
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