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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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LTEC IV
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Orphanet_93941 |
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Oromandibular dystonia
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Orphanet_93958 |
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Meige dystonia
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Orphanet_93964 |
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Meige syndrome
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Orphanet_93964 |
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Spondylometaphyseal dysplasia, 'corner fracture' type
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Orphanet_93315 |
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FHH type 1
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Orphanet_93372 |
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Syndactyly type 1
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Orphanet_93402 |
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Achondrogenesis type 1A
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Orphanet_93299 |
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Achondrogenesis type 1B
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Orphanet_93298 |
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Mucopolysaccharidosis type 1H
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Orphanet_93473 |
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Mucopolysaccharidosis type 1H/S
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Orphanet_93476 |
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Mucopolysaccharidosis type 1S
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Orphanet_93474 |
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Achondrogenesis type 2
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Orphanet_93296 |
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Brachyolmia type 2
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Orphanet_93302 |
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SEMD type 2
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Orphanet_93356 |
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