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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 mast cell leukemia
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Orphanet_566393 |
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Chronic mast cell leukemia
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Orphanet_566396 |
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Parenteral nutrition-associated cholestasis
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Orphanet_567983 |
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Aplastic desmosis coli
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Orphanet_565641 |
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Primary desmosis coli
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Orphanet_565641 |
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Heme oxygenase-1 deficiency
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Orphanet_562509 |
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Methanethiol oxidase deficiency
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Orphanet_562538 |
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Primary triglyceride deposit cardiomyovasculopathy
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Orphanet_565612 |
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Cold agglutinin disease
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Orphanet_56425 |
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Human prion disease
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Orphanet_56970 |
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Genetic systemic disease with glomerulopathy as a major feature
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Orphanet_567556 |
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Furuncular myiasis due to Cordylobia anthropophaga
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Orphanet_563687 |
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Furunculoid myiasis due to Cordylobia anthropophaga
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Orphanet_563687 |
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Furunculous myiasis due to Cordylobia anthropophaga
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Orphanet_563687 |
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Furuncular myiasis due to Cordylobia rodhaini
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Orphanet_563690 |
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