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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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Familial spastic paraplegia
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Orphanet_685 |
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Hereditary spastic paraplegia
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Orphanet_685 |
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Familial hyperkalemic periodic paralysis
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Orphanet_682 |
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Primary hyperkalemic periodic paralysis
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Orphanet_682 |
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Rare genetic skin disease
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Orphanet_68346 |
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Rare maxillo-facial surgical disease
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Orphanet_68329 |
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Amoebiasis due to free-living amoebae
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Orphanet_68 |
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Rare genetic tumor
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Orphanet_68336 |
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Rare bone tumor
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Orphanet_68411 |
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