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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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BFIE
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Orphanet_306 |
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BFIS
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Orphanet_306 |
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DYT21
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Orphanet_306734 |
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FHHNC
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Orphanet_306516 |
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Hyperekplexia
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Orphanet_306773 |
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Manganism
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Orphanet_306682 |
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Myospherulosis
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Orphanet_306553 |
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PARK9
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Orphanet_306674 |
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PHTS
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Orphanet_306498 |
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SPG1
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Orphanet_306617 |
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SPG48
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Orphanet_306511 |
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Spherulocytosis
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Orphanet_306553 |
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Snyder-Robinson syndrome
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Orphanet_3063 |
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ILNEB syndrome
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Orphanet_306504 |
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Michellis-Castrillo syndrome
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Orphanet_306516 |
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