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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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RTHb
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Orphanet_566243 |
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TGCV
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Orphanet_565612 |
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AP/AT spectum
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Orphanet_566847 |
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Hereditary ochronosis
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Orphanet_56 |
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Marshall syndrome
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Orphanet_560 |
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Marshall-Smith syndrome
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Orphanet_561 |
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FOXG1 syndrome
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Orphanet_561854 |
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McCune-Albright syndrome
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Orphanet_562 |
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HO-1 deficiency
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Orphanet_562509 |
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CLIFAHDD syndrome
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Orphanet_562528 |
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MRAMS syndrome
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Orphanet_562559 |
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Peripartum cardiomyopathy
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Orphanet_563 |
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Postpartum cardiomyopathy
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Orphanet_563 |
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Seronegative AIH
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Orphanet_563589 |
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Isolated anencephaly
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Orphanet_563609 |
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