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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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Classic granular corneal dystrophy
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Orphanet_98962 |
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Classic lattice corneal dystrophy
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Orphanet_98964 |
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Schnyder crystalline corneal dystrophy
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Orphanet_98967 |
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François-Neetens speckled corneal dystrophy
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Orphanet_98970 |
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Posterior amorphous corneal dystrophy
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Orphanet_98971 |
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Posterior polymorphous corneal dystrophy
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Orphanet_98973 |
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Fuchs endothelial corneal dystrophy
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Orphanet_98974 |
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Central cloudy corneal dystrophy of François
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Orphanet_98972 |
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Congenital fourth cranial nerve palsy
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Orphanet_98686 |
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Blake pouch cyst
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Orphanet_98922 |
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Atrioventricular canal defect
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Orphanet_98722 |
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Rare atrial defect and interatrial communication
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Orphanet_98727 |
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Congenital F8 deficiency
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Orphanet_98878 |
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Congenital FVIII deficiency
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Orphanet_98878 |
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Congenital F9 deficiency
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Orphanet_98879 |
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