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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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Genetic neuromuscular junction disease
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Orphanet_98495 |
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Climatic droplet keratopathy
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Orphanet_98958 |
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Familial paroxysmal kinesigenic dyskinesia
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Orphanet_98809 |
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Primary mediastinal large B-cell lymphoma
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Orphanet_98838 |
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Mediastinal diffuse large-cell lymphoma with sclerosis
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Orphanet_98838 |
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Chronic myelomonocytic leukemia
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Orphanet_98823 |
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Subacute myeloid leukemia
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Orphanet_98824 |
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Acute undifferentiated leukemia
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Orphanet_98835 |
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Mast cell leukemia
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Orphanet_98851 |
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Acute myeloblastic leukemia M1
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Orphanet_98833 |
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Acute myeloblastic leukemia M2
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Orphanet_98834 |
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Acute myeloid leukemia with 11q23 abnormalities
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Orphanet_98831 |
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Acute myeloblastic leukemia with maturation
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Orphanet_98834 |
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Acute myeloid leukemia with minimal differentiation
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Orphanet_98832 |
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Acute myeloid leukemia with recurrent genetic anomaly
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Orphanet_98277 |
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