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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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Acute myeloblastic leukemia without maturation
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Orphanet_98833 |
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Acute myeloid leukemia, minimal differentiation, FAB M0
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Orphanet_98835 |
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ATR syndrome linked to chromosome 16
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Orphanet_98791 |
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Adipose triglyceride lipase deficiency
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Orphanet_98908 |
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Familial partial lipodystrophy
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Orphanet_98306 |
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Familial temporal lobe epilepsy
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Orphanet_98819 |
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Large cell lymphoma of the mediastinum
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Orphanet_98838 |
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Classic Hodgkin lymphoma, lymphocyte-depleted type
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Orphanet_98846 |
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Classic Hodgkin lymphoma, lymphocyte-rich type
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Orphanet_98845 |
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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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Coloboma of macula
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Orphanet_98945 |
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Digestive tract malformation
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Orphanet_98039 |
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Posterior fossa malformation
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Orphanet_98519 |
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Congenital tricuspid malformation
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Orphanet_98721 |
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