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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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Infant-like botulism
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Orphanet_178487 |
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Perry syndrome
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Orphanet_178509 |
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Berti lymphoma
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Orphanet_178528 |
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Opitz-Caltabiano syndrome
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Orphanet_1786 |
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Acquired neutropenia
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Orphanet_178996 |
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Immunologic neutropenia
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Orphanet_178996 |
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Primary cutaneous B-cell lymphoma
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Orphanet_178563 |
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Acrofacial dysostosis, Catania type
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Orphanet_1786 |
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Acrofacial dysostosis, Palagonia type
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Orphanet_1787 |
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Brain calcification, Rajab type
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Orphanet_178506 |
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Acrofacial dysostosis, RodrÃguez type
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Orphanet_1788 |
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Pagetoid reticulosis, Woringer-Kolopp type
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Orphanet_178517 |
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Primary cutaneous aggressive epidermotropic CD8+ T-cell lymphoma
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Orphanet_178528 |
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Parkinsonism with alveolar hypoventilation and mental depression
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Orphanet_178509 |
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Mycosis fungoides and variants
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Orphanet_178566 |
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