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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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Peroxisomal disease
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Orphanet_68373 |
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Mitochondrial disease
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Orphanet_68380 |
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Neuromuscular disease
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Orphanet_68381 |
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Neurometabolic disease
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Orphanet_68385 |
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Paramyotonia congenita
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Orphanet_684 |
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Strümpell-Lorrain disease
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Orphanet_685 |
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Gamstorp episodic adynamy
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Orphanet_682 |
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Multiple congenital anomalies/dysmorphic syndrome
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Orphanet_68341 |
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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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Rare vascular disease
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Orphanet_68362 |
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Rare metabolic disease
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Orphanet_68367 |
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Rare infectious disease
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Orphanet_68416 |
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