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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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Early-onset anterior polar cataract
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Orphanet_98988 |
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Early-onset posterior polar cataract
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Orphanet_98993 |
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Bilateral perisylvian polymicrogyria
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Orphanet_98889 |
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Acute inflammatory polyneuropathy
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Orphanet_98916 |
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Aplasia of pulmonary artery
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Orphanet_980 |
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Transient acquired pure red cell aplasia
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Orphanet_98871 |
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Primary acquired pure red cell aplasia
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Orphanet_98872 |
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AML with recurrent genetic anomaly
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Orphanet_98277 |
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Primary acquired red cell aplasia
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Orphanet_98421 |
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Primary autoimmune red cell aplasia
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Orphanet_98421 |
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Embryonic testicular regression syndrome
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Orphanet_983 |
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Rare genetic renal disease
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Orphanet_98056 |
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Rare allergic respiratory disease
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Orphanet_98052 |
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Autosomal dominant sleep-related hypermotor epilepsy
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Orphanet_98784 |
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Autosomal recessive spastic ataxia of Charlevoix-Saguenay
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Orphanet_98 |
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