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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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Acrofacial dysostosis, Kennedy-Teebi type
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Orphanet_64542 |
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Lipomatous flat LDM
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Orphanet_645300 |
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Lipomatous non-saccular LDM
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Orphanet_645300 |
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Fibroneural flat LDM
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Orphanet_645310 |
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Fibroneural non-saccular LDM
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Orphanet_645310 |
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Granuloma of Lever
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Orphanet_615943 |
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Hemophilia B Leyden
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Orphanet_617930 |
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F9 deficiency, Leyden type
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Orphanet_617930 |
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Follicular T-cell Lymphoma
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Orphanet_652650 |
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Distal myopathy, Nonaka type
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Orphanet_602 |
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Preaxial brachydactyly, PAX3 type
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Orphanet_633211 |
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Fragile X-associated POF
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Orphanet_642691 |
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Fragile X-associated POI
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Orphanet_642691 |
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Atrophoderma of Pasini and Pierini
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Orphanet_658810 |
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Alpha-sarcoglycan-related LGMD R3
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Orphanet_62 |
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