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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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Granular corneal dystrophy type 2
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Orphanet_98963 |
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Granular corneal dystrophy type 3
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Orphanet_98961 |
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Granular corneal dystrophy type I
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Orphanet_98962 |
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Lattice corneal dystrophy type I
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Orphanet_98964 |
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Granular corneal dystrophy type II
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Orphanet_98963 |
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Granular corneal dystrophy type III
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Orphanet_98961 |
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Late hereditary endothelial dystrophy
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Orphanet_98974 |
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Cogan microcystic epithelial dystrophy
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Orphanet_98956 |
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Juvenile hereditary epithelial dystrophy of Meesmann
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Orphanet_98954 |
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Coloboma of eye lens
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Orphanet_98943 |
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Coloboma of eyelid
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Orphanet_98946 |
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Primary congenital glaucoma
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Orphanet_98976 |
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Coloboma of iris
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Orphanet_98944 |
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Climatic droplet keratopathy
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Orphanet_98958 |
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Adipose triglyceride lipase deficiency
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Orphanet_98908 |
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