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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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APML
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Orphanet_520 |
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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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Ulnar/fibula ray defect-brachydactyly syndrome
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Orphanet_52056 |
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Proximal 11p deletion syndrome
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Orphanet_52022 |
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Acute promyelocytic leukemia
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Orphanet_520 |
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Acute myeloblastic leukemia 3
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Orphanet_520 |
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Rare disorder of the visual organs
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Orphanet_520814 |
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Progressive external ophthalmoplegia
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Orphanet_520820 |
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Isolated inherited retinal disorder
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Orphanet_520817 |
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