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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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Illum syndrome
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Orphanet_1150 |
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Oculomelic amyoplasia
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Orphanet_1154 |
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Beckwith-Wiedemann syndrome
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Orphanet_116 |
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Exomphalos-macroglossia-gigantism syndrome
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Orphanet_116 |
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Wiedemann-Beckwith syndrome
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Orphanet_116 |
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Chylous ascites
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Orphanet_1160 |
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Allergic aspergillosis
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Orphanet_1164 |
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Hinson-Pepys disease
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Orphanet_1164 |
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Behçet disease
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Orphanet_117 |
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CAPOS syndrome
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Orphanet_1171 |
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Gordon-Holmes syndrome
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Orphanet_1173 |
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Harding ataxia
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Orphanet_1177 |
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Ouvrier-Billson syndrome
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Orphanet_1179 |
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Beta-mannosidase deficiency
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Orphanet_118 |
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Boucher-Neuhäuser syndrome
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Orphanet_1180 |
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