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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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Rare genetic cardiac disease
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Orphanet_98054 |
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Early-onset sutural cataract
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Orphanet_98985 |
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Early-onset nuclear cataract
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Orphanet_98991 |
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Early-onset partial cataract
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Orphanet_98992 |
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Total early-onset cataract
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Orphanet_98994 |
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Early-onset zonular cataract
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Orphanet_98995 |
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Anterior horn cell disease
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Orphanet_98503 |
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Angiotropic large cell lymphoma
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Orphanet_98839 |
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Anaplastic large cell lymphoma
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Orphanet_98841 |
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Autosomal recessive cerebellar ataxia due to a DNA repair defect
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Orphanet_98097 |
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Rare genetic disease
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Orphanet_98053 |
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Autoimmune neurological channelopathy
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Orphanet_98750 |
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Genetic neurological channelopathy of the central nervous system
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Orphanet_98743 |
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Early-onset benign childhood occipital epilepsy
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Orphanet_98815 |
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Late-onset benign childhood occipital epilepsy
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Orphanet_98816 |
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