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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.
Congenital symblepharon
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Orphanet_98948 |
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Complete cryptophthalmia
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Orphanet_98949 |
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Partial cryptophthalmia
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Orphanet_98950 |
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Map-dot-fingerprint dystrophy
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Orphanet_98956 |
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Classic GCD
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Orphanet_98962 |
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Biber-Haab-Dimmer dystrophy
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Orphanet_98964 |
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Schlichting dystrophy
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Orphanet_98973 |
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Congenital glaucoma
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Orphanet_98976 |
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Juvenile glaucoma
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Orphanet_98977 |
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Axenfeld anomaly
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Orphanet_98978 |
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Chandler syndrome
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Orphanet_98979 |
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Cogan-Reese syndrome
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Orphanet_98980 |
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Coppock-like cataract
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Orphanet_98984 |
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Dusty cataract
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Orphanet_98984 |
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Pulverulent cataract
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Orphanet_98984 |
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