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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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Adenomucinosis
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Orphanet_26790 |
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LGMD2A
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Orphanet_267 |
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MADD
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Orphanet_26791 |
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SCADD
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Orphanet_26792 |
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VLCADD
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Orphanet_26793 |
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Primary calpainopathy
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Orphanet_267 |
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Pierson syndrome
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Orphanet_2670 |
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Neu-Laxova syndrome
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Orphanet_2671 |
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Neuhauser-Eichner-Opitz syndrome
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Orphanet_2672 |
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Neurofaciodigitorenal syndrome
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Orphanet_2673 |
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Gelatinous ascites
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Orphanet_26790 |
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Pseudomyxoma peritonei
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Orphanet_26790 |
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MAD deficiency
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Orphanet_26791 |
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ACADS deficiency
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Orphanet_26792 |
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SCAD deficiency
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Orphanet_26792 |
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