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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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Hemolytic uremic syndrome
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Orphanet_544458 |
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PRUNE1-related neurological syndrome
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Orphanet_544469 |
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Atypical Fanconi syndrome-neonatal hyperinsulinism syndrome
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Orphanet_544628 |
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Infection-related hemolytic uremic syndrome
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Orphanet_544482 |
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Atypical HUS with complement gene abnormality
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Orphanet_544472 |
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Congenital myopathy with fast-twitch fiber atrophy
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Orphanet_544602 |
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Congenital myopathy with reduced type 2 muscle fibers
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Orphanet_544602 |
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Congenital myopathy with reduced type II muscle fibers
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Orphanet_544602 |
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Congenital myopathy with type 2 muscle fiber atrophy
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Orphanet_544602 |
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Congenital myopathy with type II fiber atrophy
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Orphanet_544602 |
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