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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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PKAN
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Orphanet_157850 |
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SCD-EDS
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Orphanet_157965 |
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spEDS-SLC39A13
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Orphanet_157965 |
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Knobloch syndrome
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Orphanet_1571 |
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Knobloch-Layer syndrome
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Orphanet_1571 |
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Primary hypogammaglobulinemia
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Orphanet_1572 |
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Mackay-Shek-Carr syndrome
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Orphanet_1574 |
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Situs ambiguous
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Orphanet_157769 |
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Situs ambiguus
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Orphanet_157769 |
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Epithelioid hemangioendothelioma
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Orphanet_157791 |
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Klüver-Bucy syndrome
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Orphanet_157823 |
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Congenital epulis
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Orphanet_157826 |
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Neumann tumor
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Orphanet_157826 |
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Paroxysmal hemicrania
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Orphanet_157835 |
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Ferritin-related neurodegeneration
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Orphanet_157846 |
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