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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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LP pigmentosus
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Orphanet_254463 |
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LP pemphigoides
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Orphanet_254478 |
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Inhalation botulism
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Orphanet_254504 |
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Inhalational botulism
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Orphanet_254504 |
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Iatrogenic botulism
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Orphanet_254509 |
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Inadvertent botulism
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Orphanet_254509 |
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Temple syndrome
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Orphanet_254516 |
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Kagami-Ogata syndrome
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Orphanet_254519 |
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Paternal del(14)(q32.2)
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Orphanet_254525 |
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Maternal del(14)(q32.2)
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Orphanet_254528 |
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Thomas-Jewett-Raines syndrome
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Orphanet_2547 |
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Benign hyperferritinemia
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Orphanet_254704 |
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mtDNA-related dystonia
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Orphanet_254851 |
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Deafness-encephaloneuropathy-obesity-valvulopathy syndrome
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Orphanet_254898 |
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Moeschler-Clarren syndrome
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Orphanet_2549 |
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