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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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Mulibrey growth disorder
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Orphanet_2576 |
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Spastic ataxia-corneal dystrophy syndrome
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Orphanet_2572 |
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EBS with muscular dystrophy
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Orphanet_257 |
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Epidermolysis bullosa simplex with muscular dystrophy
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Orphanet_257 |
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Lubani-Al Saleh-Teebi syndrome
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Orphanet_2575 |
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Atypical MRKH syndrome
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Orphanet_2578 |
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MRKH syndrome type 2
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Orphanet_2578 |
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Mayer-Rokitansky-Küster-Hauser syndrome type 2
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Orphanet_2578 |
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