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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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Classic pyoderma gangrenosum
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Orphanet_538863 |
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Ulcerative pyoderma gangrenosum
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Orphanet_538863 |
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Pustular pyoderma gangrenosum
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Orphanet_538866 |
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Bullous pyoderma gangrenosum
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Orphanet_538869 |
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Phemphigoid pyoderma gangrenosum
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Orphanet_538869 |
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Granulomatous pyoderma gangrenosum
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Orphanet_538872 |
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Vegetative pyoderma gangrenosum
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Orphanet_538872 |
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Rare cutaneous lupus erythematosus
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Orphanet_535 |
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Familial lipase maturation factor 1 deficiency
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Orphanet_535453 |
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Spinal arteriovenous metameric syndrome
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Orphanet_53721 |
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Cerebrofacial arteriovenous metameric syndrome type 2
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Orphanet_53719 |
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Distal hereditary motor neuropathy
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Orphanet_53739 |
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Distal spinal muscular atrophy
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Orphanet_53739 |
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Hereditary chin myoclonus
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Orphanet_53372 |
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Hyaline body myopathy
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Orphanet_53698 |
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