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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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PHHI
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Orphanet_657 |
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Paragonimiasis
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Orphanet_658913 |
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RION
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Orphanet_659634 |
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SION
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Orphanet_659626 |
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SVCA
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Orphanet_652668 |
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iSGS
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Orphanet_652681 |
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nTFHL-F
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Orphanet_652650 |
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LCAT deficiency
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Orphanet_650 |
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Rare CPP
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Orphanet_650063 |
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Genetic CPP
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Orphanet_650182 |
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Wermer syndrome
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Orphanet_652 |
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Carvajal syndrome
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Orphanet_65282 |
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Timothy syndrome
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Orphanet_65283 |
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Lhermitte-Duclos disease
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Orphanet_65285 |
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3qter deletion
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Orphanet_65286 |
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