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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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Aprosencephaly
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Orphanet_566857 |
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Atelencephaly
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Orphanet_566852 |
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CAIN
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Orphanet_566067 |
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CARST
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Orphanet_566192 |
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RTHa
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Orphanet_566231 |
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RTHb
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Orphanet_566243 |
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AP/AT spectum
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Orphanet_566847 |
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Congenital microcoria
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Orphanet_566 |
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Congenital miosis
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Orphanet_566 |
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CD55 deficiency
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Orphanet_566175 |
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CHAPLE syndrome
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Orphanet_566175 |
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Acute MCL
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Orphanet_566393 |
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Chronic MCL
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Orphanet_566396 |
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Hepatic adenomatosis
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Orphanet_566841 |
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Liver adenomatosis
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Orphanet_566841 |
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