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| created at |
2024-09-23 16:23:50 UTC |
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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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Curry-Hall syndrome
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Orphanet_952 |
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PAFAH1B1-related lissencephaly
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Orphanet_95232 |
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Acrofacial dysostosis, Weyers type
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Orphanet_952 |
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Weyers acrodental dysostosis
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Orphanet_952 |
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Weyers acrofacial dysostosis
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Orphanet_952 |
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Lissencephaly due to LIS1 mutation
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Orphanet_95232 |
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