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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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CISS
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Orphanet_157820 |
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Craniorhiny
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Orphanet_157832 |
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MSSD
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Orphanet_157801 |
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NBIA1
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Orphanet_157850 |
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Neuroferritinopathy
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Orphanet_157846 |
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PKAN
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Orphanet_157850 |
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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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Hereditary ferritinopathy
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Orphanet_157846 |
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Hallervorden-Spatz syndrome
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Orphanet_157850 |
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Syndactyly type 9
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Orphanet_157801 |
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Neurodegeneration with brain iron accumulation type 1
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Orphanet_157850 |
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