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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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Genochondromatosis type 2
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Orphanet_93398 |
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Syndactyly type 2
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Orphanet_93403 |
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Brachyolmia type 3
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Orphanet_93304 |
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Syndactyly type 3
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Orphanet_93404 |
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Syndactyly type 4
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Orphanet_93405 |
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Syndactyly type 5
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Orphanet_93406 |
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Cystinuria type A
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Orphanet_93612 |
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Brachydactyly type A1
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Orphanet_93388 |
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Brachydactyly type A2
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Orphanet_93396 |
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Brachydactyly type A4
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Orphanet_93394 |
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Brachydactyly type A6
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Orphanet_93382 |
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Brachydactyly type A7
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Orphanet_93397 |
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XDH and AOX dual deficiency
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Orphanet_93602 |
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Spondylometaphyseal dysplasia, Algerian type
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Orphanet_93316 |
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Brachydactyly type B
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Orphanet_93383 |
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