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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.
Erythema elevatum diutinum
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Orphanet_90000 |
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Invasive infections due to VRE
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Orphanet_90078 |
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46,XY DSD due to a testosterone synthesis defect
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Orphanet_90783 |
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46,XY DSD due to adrenal and testicular steroidogenesis defect
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Orphanet_90786 |
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Congenital polycythemia due to erythropoietin receptor mutation
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Orphanet_90042 |
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Hemolytic anemia due to glutathione reductase deficiency
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Orphanet_90030 |
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46,XY DSD due to testicular steroidogenesis defect
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Orphanet_90787 |
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Invasive infections due to vancomycin-resistant enterococci
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Orphanet_90078 |
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X-linked cone dysfunction syndrome with myopia
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Orphanet_90001 |
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Telangiectasia macularis eruptiva perstans
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Orphanet_90389 |
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Discoid lupus erythematosus
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Orphanet_90281 |
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Primary congenital erythrocytosis
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Orphanet_90042 |
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Acute hepatic failure
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Orphanet_90062 |
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Acute liver failure
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Orphanet_90062 |
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Fulminant hepatic failure
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Orphanet_90062 |
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