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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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Oculotrichodysplasia
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Orphanet_2718 |
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hATTR
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Orphanet_271861 |
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ATTRv amyloidosis
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Orphanet_271861 |
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Cecato de Lima-Pinheiro syndrome
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Orphanet_2718 |
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Hereditary TTR amyloid polyneuropathy
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Orphanet_271861 |
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Hereditary transthyretin amyloid polyneuropathy
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Orphanet_271861 |
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Familial TTR-related amyloidosis
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Orphanet_271861 |
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Familial transthyretin-related amyloidosis
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Orphanet_271861 |
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Hereditary ATTR amyloidosis
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Orphanet_271861 |
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Hereditary TTR amyloidosis
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Orphanet_271861 |
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Genetic cardiac anomaly
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Orphanet_271853 |
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Rare genetic systemic or rheumatologic disease
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Orphanet_271870 |
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Genetic soft tissue tumor
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Orphanet_271832 |
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Genetic digestive tract tumor
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Orphanet_271835 |
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Genetic mesenchymal tumor
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Orphanet_271832 |
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