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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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Pediatric multiple sclerosis
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Orphanet_477738 |
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Genetic cerebral small vessel disease
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Orphanet_477754 |
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17p11.2p12 microduplication syndrome
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Orphanet_477817 |
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Kosaki overgrowth syndrome
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Orphanet_477831 |
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Syndromic constitutional thrombocytopenia
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Orphanet_477794 |
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Isolated constitutional thrombocytopenia
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Orphanet_477797 |
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Non-syndromic constitutional thrombocytopenia
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Orphanet_477797 |
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Rare disorder with a moyamoya angiopathy
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Orphanet_477771 |
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