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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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SJS1
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Orphanet_800 |
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Aberfeld syndrome
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Orphanet_800 |
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Burton syndrome
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Orphanet_800 |
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Catel-Hempel syndrome
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Orphanet_800 |
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Myotonic chondrodystrophy
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Orphanet_800 |
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Osteochondromuscular dystrophy
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Orphanet_800 |
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Schwartz-Jampel syndrome
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Orphanet_800 |
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Schwartz-Jampel-Aberfeld syndrome
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Orphanet_800 |
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Burton skeletal dysplasia
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Orphanet_800 |
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Dysostosis enchondralis metaepiphysaria, Catel-Hempel type
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Orphanet_800 |
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Schwartz-Jampel syndrome type 1
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Orphanet_800 |
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