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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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Pierquin syndrome
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Orphanet_1566 |
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Rare genetic cause of hypertension
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Orphanet_156629 |
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Rare genetic endocrine disease
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Orphanet_156638 |
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Genetic endocrine growth disease
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Orphanet_156643 |
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Rare genetic hepatic disease
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Orphanet_156601 |
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Genetic parenchymatous liver disease
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Orphanet_156604 |
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Dandy-Walker malformation-postaxial polydactyly syndrome
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Orphanet_1566 |
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DWM with postaxial polydactyly
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Orphanet_1566 |
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Rare genetic respiratory disease
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Orphanet_156610 |
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Genetic biliary tract disease
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Orphanet_156607 |
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Genetic urogenital tract malformation
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Orphanet_156622 |
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Rare genetic urogenital disease
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Orphanet_156619 |
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