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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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Multiple congenital anomalies/dysmorphic syndrome
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Orphanet_68341 |
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Fibrolipomatous filum anomaly
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Orphanet_645279 |
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Rare maxillofacial anomaly
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Orphanet_68329 |
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Rare chromosomal anomaly
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Orphanet_68335 |
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Rare vascular anomaly
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Orphanet_68419 |
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Rare constitutional aplastic anemia
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Orphanet_68383 |
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Isolated retinal arteriovenous aneurysm 3
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Orphanet_674924 |
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Central retinal artery occlusion
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Orphanet_648684 |
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Isolated pulmonary artery sling
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Orphanet_658574 |
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Superior mesenteric artery syndrome
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Orphanet_622099 |
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Familial recurrent arthritis
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Orphanet_69126 |
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Mandibuloacral dysplasia associated to MTX2
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Orphanet_647667 |
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Classic pilocytic astrocytoma
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Orphanet_673580 |
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Juvenile pilocytic astrocytoma
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Orphanet_673580 |
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Anaplastic pilocytic astrocytoma
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Orphanet_673585 |
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