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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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Chung-Jansen syndrome
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Orphanet_589905 |
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Mucopolysaccharidosis type 2
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Orphanet_580 |
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Mucopolysaccharidosis type 3
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Orphanet_581 |
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Mucopolysaccharidosis type 4
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Orphanet_582 |
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Mucopolysaccharidosis type 6
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Orphanet_583 |
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Mucopolysaccharidosis type 7
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Orphanet_584 |
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Philadelphia chromosome-like B-ALL
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Orphanet_585909 |
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AML with BCR-ABL1
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Orphanet_585867 |
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GRIN2B-Related Neurodevelopmental Disorder
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Orphanet_589547 |
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Mucopolysaccharidosis type II
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Orphanet_580 |
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Mucopolysaccharidosis type III
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Orphanet_581 |
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Mucopolysaccharidosis type IV
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Orphanet_582 |
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Mucopolysaccharidosis type VI
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Orphanet_583 |
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Mucopolysaccharidosis type VII
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Orphanet_584 |
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Mixed phenotype acute leukemia with t(9;22)(q34.1;q11.2)
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Orphanet_589534 |
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