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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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EEC syndrome and related syndrome
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Orphanet_98609 |
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Acute motor and sensory axonal neuropathy
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Orphanet_98917 |
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Generalized cervical and upper-limb-onset dystonia
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Orphanet_98806 |
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Constitutional sideroblastic anemia
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Orphanet_98362 |
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Rare hemolytic anemia
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Orphanet_98363 |
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Autoimmune hemolytic anemia
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Orphanet_98375 |
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Constitutional hemolytic anemia due to acanthocytic disorder
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Orphanet_98366 |
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Constitutional hemolytic anemia due to acanthocytosis
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Orphanet_98366 |
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Congenital dyserythropoietic anemia type 1
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Orphanet_98869 |
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Congenital dyserythropoietic anemia type 2
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Orphanet_98873 |
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Congenital dyserythropoietic anemia type 3
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Orphanet_98870 |
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Congenital dyserythropoietic anemia type I
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Orphanet_98869 |
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Congenital dyserythropoietic anemia type II
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Orphanet_98873 |
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Congenital dyserythropoietic anemia type III
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Orphanet_98870 |
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Allosome number anomaly
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Orphanet_98156 |
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