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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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Nijmegen breakage syndrome
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Orphanet_647 |
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Iridocorneal endothelial syndrome
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Orphanet_64734 |
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Ovarian hyperstimulation syndrome
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Orphanet_64739 |
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Nevus comedonicus syndrome
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Orphanet_64754 |
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Becker naevus syndrome
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Orphanet_64755 |
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Becker nevus syndrome
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Orphanet_64755 |
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Adrenal Cushing syndrome
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Orphanet_647758 |
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MYT1L-related Prader-Willi-like syndrome
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Orphanet_647799 |
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Idiopathic catatonic syndrome
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Orphanet_648919 |
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Isolated catatonic syndrome
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Orphanet_648919 |
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Central nervous system tuberculosis
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Orphanet_641396 |
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Anomaly of the filum
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Orphanet_645282 |
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Lipoma of the filum terminale
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Orphanet_645325 |
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Bartonellosis due to Bartonella quintana infection
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Orphanet_64694 |
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HAFOUS due to USP7 mutation
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Orphanet_643538 |
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