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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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DIDOD
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Orphanet_589905 |
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DYT28
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Orphanet_589618 |
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SCA45
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Orphanet_589527 |
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SCA46
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Orphanet_589522 |
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Acquired myasthenia
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Orphanet_589 |
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Myasthenia gravis
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Orphanet_589 |
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Liberfarb syndrome
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Orphanet_589442 |
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PADDAS syndrome
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Orphanet_589515 |
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Dystonia 28
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Orphanet_589618 |
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KMT2B-related dystonia
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Orphanet_589618 |
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Chung-Jansen syndrome
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Orphanet_589905 |
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GRIN2B-Related Neurodevelopmental Disorder
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Orphanet_589547 |
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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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Mixed phenotype acute leukemia with t(v;11q23.3)
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Orphanet_589595 |
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Myeloid/lymphoid neoplasm associated with JAK2 rearrangement
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Orphanet_589542 |
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