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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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Isochromosomy Yq
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Orphanet_98798 |
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GTPCH1-deficient DRD
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Orphanet_98808 |
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Familial PKD
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Orphanet_98809 |
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Dystonia 18
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Orphanet_98811 |
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Panayiotopoulos syndrome
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Orphanet_98815 |
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Landau-Kleffner syndrome
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Orphanet_98818 |
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Refractory anemia
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Orphanet_98826 |
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AML M0
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Orphanet_98832 |
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AML M1
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Orphanet_98833 |
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AML M2
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Orphanet_98834 |
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Intravascular lymphomatosis
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Orphanet_98839 |
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Malignant angioendotheliomatosis
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Orphanet_98839 |
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Tappeiner-Pfleger disease
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Orphanet_98839 |
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Lymphomatoid papulosis
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Orphanet_98842 |
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Hereditary ovalocytosis
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Orphanet_98868 |
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