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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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Congenital Factor VIII deficiency
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Orphanet_98878 |
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Minimally differentiated acute myeloblastic leukemia
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Orphanet_98832 |
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CD30 positive anaplastic large cell lymphoma
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Orphanet_98841 |
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Ki-1 positive anaplastic large cell lymphoma
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Orphanet_98841 |
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Generalized cervical and upper-limb-onset dystonia
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Orphanet_98806 |
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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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Acquired epileptic aphasia
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Orphanet_98818 |
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Autosomal recessive axonal CMT4C1
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Orphanet_98856 |
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Angiotropic large cell lymphoma
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Orphanet_98839 |
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Anaplastic large cell lymphoma
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Orphanet_98841 |
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