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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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Classic Hodgkin lymphoma, mixed cellularity type
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Orphanet_98844 |
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Classic Hodgkin lymphoma, nodular sclerosis type
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Orphanet_98843 |
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HPD with marked diurnal fluctuation
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Orphanet_98808 |
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Indolent systemic mastocytosis
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Orphanet_98848 |
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Aggressive systemic mastocytosis
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Orphanet_98850 |
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X-linked Emery-Dreifuss muscular dystrophy
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Orphanet_98863 |
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Unclassified mixed myelodysplastic/myeloproliferatic syndrome
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Orphanet_98825 |
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Atypical chronic myeloid leukemia
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Orphanet_98824 |
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Oculopharyngeal distal myopathy
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Orphanet_98897 |
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Benign childhood occipital epilepsy, Gastaut type
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Orphanet_98816 |
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Benign childhood occipital epilepsy, Panayiotopoulos type
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Orphanet_98815 |
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Transient erythroblastopenia of childhood
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Orphanet_98871 |
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Early-onset X-linked optic atrophy
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Orphanet_98890 |
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Non-Leber type optic atrophy with early-onset
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Orphanet_98890 |
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Southeast Asian ovalocytosis
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Orphanet_98868 |
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