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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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Mucopolysaccharidosis type I
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Orphanet_579 |
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Atelosteogenesis type II
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Orphanet_56304 |
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SCM type II
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Orphanet_573253 |
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Mucolipidosis type II
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Orphanet_576 |
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Mucopolysaccharidosis type II
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Orphanet_580 |
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Mucolipidosis type II alpha/beta
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Orphanet_576 |
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MHC class II deficiency
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Orphanet_572 |
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Atelosteogenesis type III
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Orphanet_56305 |
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Mucolipidosis type III
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Orphanet_577 |
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Mucopolysaccharidosis type III
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Orphanet_581 |
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Mucolipidosis type IV
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Orphanet_578 |
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Mucopolysaccharidosis type IV
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Orphanet_582 |
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Acquired factor IX deficiency
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Orphanet_599485 |
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Serotonin-producing pancreatic NET
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Orphanet_506090 |
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Primary cutaneous Ki-1+ T-cell lymphoproliferative disease
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Orphanet_541 |
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