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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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Retinal dystrophy
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Orphanet_71862 |
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Muscular channelopathy
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Orphanet_71864 |
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Isolated Pierre Robin sequence
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Orphanet_718 |
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Isolated Pierre Robin syndrome
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Orphanet_718 |
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Inherited retinal disorder
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Orphanet_71862 |
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Rare genetic neurological disorder
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Orphanet_71859 |
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