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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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ALPS
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Orphanet_3261 |
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Parahemophilia
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Orphanet_326 |
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Owren disease
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Orphanet_326 |
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Proaccelerin deficiency
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Orphanet_326 |
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Canale-Smith syndrome
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Orphanet_3261 |
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Dobrow syndrome
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Orphanet_3262 |
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Giuffré-Tsukahara syndrome
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Orphanet_3268 |
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Tsukahara syndrome
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Orphanet_3268 |
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Congenital factor V deficiency
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Orphanet_326 |
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Isolated congenital humero-radioulnar fusion
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Orphanet_3266 |
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Isolated congenital humeroradial fusion
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Orphanet_3265 |
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Isolated congenital radioulnar fusion
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Orphanet_3269 |
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Idiopathic hypereosinophilic syndrome
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Orphanet_3260 |
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Autoimmune lymphoproliferative syndrome
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Orphanet_3261 |
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Syngnathia-multiple anomalies syndrome
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Orphanet_3262 |
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