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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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Wyburn-Mason syndrome
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Orphanet_53719 |
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Cobb syndrome
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Orphanet_53721 |
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Cutaneomeningospinal angiomatosis
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Orphanet_53721 |
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SAMS 1-31
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Orphanet_53721 |
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ITK deficiency
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Orphanet_538963 |
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Familial HLH
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Orphanet_540 |
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Kelly-Paterson syndrome
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Orphanet_54028 |
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Plummer-Vinson syndrome
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Orphanet_54028 |
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Sideropenic dysphagia
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Orphanet_54028 |
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Moschcowitz disease
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Orphanet_54057 |
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Labrune syndrome
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Orphanet_542310 |
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Benson syndrome
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Orphanet_54247 |
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Necrobiosis lipoidica
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Orphanet_542592 |
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Oppenheim-Urbach disease
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Orphanet_542592 |
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Spongy myocardium
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Orphanet_54260 |
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