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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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SPAX8
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Orphanet_527497 |
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Vasculitis
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Orphanet_52759 |
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cHCC-CC
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Orphanet_529852 |
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Alagille syndrome
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Orphanet_52 |
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Alagille-Watson syndrome
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Orphanet_52 |
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Arteriohepatic dysplasia
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Orphanet_52 |
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AML M3
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Orphanet_520 |
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11p11.2 deletion
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Orphanet_52022 |
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Potocki-Shaffer syndrome
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Orphanet_52022 |
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Braddock syndrome
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Orphanet_52047 |
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Longman-Tolmie syndrome
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Orphanet_52054 |
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Graham-Cox syndrome
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Orphanet_52055 |
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Morava-Mehes syndrome
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Orphanet_52056 |
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Radiation-induced plexopathy
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Orphanet_521123 |
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Radiation-induced disorder
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Orphanet_521132 |
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