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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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FACAS
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Orphanet_617919 |
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TAPS
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Orphanet_617294 |
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TRAP
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Orphanet_617297 |
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sFGR
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Orphanet_617301 |
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sIUGR
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Orphanet_617301 |
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Classic EPF
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Orphanet_617408 |
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Ofuji disease
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Orphanet_617408 |
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PLMT syndrome
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Orphanet_617440 |
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Conjunctival melanoma
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Orphanet_617910 |
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Hemophilia B Leyden
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Orphanet_617930 |
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F9 deficiency, Leyden type
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Orphanet_617930 |
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Painful legs and moving toes syndrome
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Orphanet_617440 |
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F12-associated cold autoinflammatory syndrome
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Orphanet_617919 |
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Factor IX deficiency, Leyden type
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Orphanet_617930 |
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Rare disorder due to inadequate sharing of the placenta
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Orphanet_617313 |
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