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| created at |
2024-09-23 16:23:50 UTC |
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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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Familial HLH
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Orphanet_540 |
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Kelly-Paterson syndrome
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Orphanet_54028 |
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Plummer-Vinson syndrome
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Orphanet_54028 |
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Sideropenic dysphagia
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Orphanet_54028 |
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Moschcowitz disease
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Orphanet_54057 |
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Familial hemophagocytic lymphohistiocytosis
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Orphanet_540 |
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Thrombotic thrombocytopenic purpura
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Orphanet_54057 |
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