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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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Jejunal neuroendocrine tumor
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Orphanet_100077 |
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Ileal neuroendocrine tumor
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Orphanet_100078 |
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Rectal neuroendocrine tumor
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Orphanet_100081 |
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Laryngeal neuroendocrine tumor
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Orphanet_100083 |
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Gallbladder neuroendocrine tumor
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Orphanet_100086 |
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Rare thyroid tumor
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Orphanet_100087 |
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Rare parathyroid tumor
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Orphanet_100090 |
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Multiple polyglandular tumor
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Orphanet_100094 |
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HCHWA, Dutch type
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Orphanet_100006 |
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HCHWA, Icelandic type
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Orphanet_100008 |
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Amelogenesis imperfecta type 1
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Orphanet_100031 |
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Hereditary angioedema type 1
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Orphanet_100050 |
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Acquired angioedema type 1
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Orphanet_100056 |
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Amelogenesis imperfecta type 2
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Orphanet_100033 |
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Hereditary angioedema type 2
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Orphanet_100051 |
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