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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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MIS-C/A
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Orphanet_598363 |
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MmD
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Orphanet_598 |
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UTUC
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Orphanet_598216 |
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Multiminicore disease
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Orphanet_598 |
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Multiminicore myopathy
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Orphanet_598 |
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FHEIG syndrome
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Orphanet_598603 |
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Transitional cell carcinoma of the pelvis and ureter
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Orphanet_598216 |
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Transitional cell carcinoma of the upper urinary tract
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Orphanet_598216 |
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FOXG1 syndrome due to intragenic alteration
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Orphanet_598164 |
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Multisystem inflammatory syndrome in children and adults
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Orphanet_598363 |
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Upper tract urothelial carcinoma
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Orphanet_598216 |
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