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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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Brachydactyly, Farabee type
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Orphanet_93388 |
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Brachydactyly, Temtamy type
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Orphanet_93394 |
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Brachydactyly, Mohr-Wriedt type
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Orphanet_93396 |
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Brachydactyly, Smorgasbord type
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Orphanet_93397 |
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Polysyndactyly, Haas type
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Orphanet_93405 |
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Brachydactyly-syndactyly, Zhao type
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Orphanet_93409 |
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Pfeiffer syndrome type 1
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Orphanet_93258 |
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Polyepiphyseal dysplasia type 1
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Orphanet_93308 |
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Preaxial polydactyly type 1
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Orphanet_93339 |
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Primary hyperoxaluria type 1
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Orphanet_93598 |
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Dent disease type 1
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Orphanet_93622 |
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FG syndrome type 1
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Orphanet_93932 |
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Laryngo-tracheo-esophageal cleft type 1
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Orphanet_93938 |
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Laryngotracheoesophageal cleft type 1
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Orphanet_93938 |
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Pfeiffer syndrome type 2
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Orphanet_93259 |
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