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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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Acquired angioneurotic edema type 2
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Orphanet_100055 |
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Hereditary angioneurotic edema type 3
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Orphanet_100054 |
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Hereditary cerebral hemorrhage with amyloidosis, Dutch type
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Orphanet_100006 |
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Hereditary cerebral hemorrhage with amyloidosis, Icelandic type
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Orphanet_100008 |
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Bathing suit ichthyosis
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Orphanet_100976 |
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Hypoplastic amelogenesis imperfecta
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Orphanet_100031 |
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Hypocalcified amelogenesis imperfecta
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Orphanet_100032 |
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Hypomaturation amelogenesis imperfecta
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Orphanet_100033 |
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Immunoproliferative small intestinal disease
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Orphanet_100025 |
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Trisomy 3 mosaicism
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Orphanet_100071 |
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Hepatic solitary necrotic nodule
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Orphanet_100035 |
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Jejunal neuroendocrine neoplasm
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Orphanet_100077 |
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Ileal neuroendocrine neoplasm
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Orphanet_100078 |
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Appendiceal neuroendocrine neoplasm
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Orphanet_100079 |
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Gastroenteropancreatic neuroendocrine neoplasm
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Orphanet_100092 |
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