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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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22q11DS
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Orphanet_567 |
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PNAC
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Orphanet_567983 |
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Genetic systemic disease with glomerulopathy as a major feature
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Orphanet_567556 |
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Systemic vasculitis associated with glomerulopathy
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Orphanet_567560 |
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Idiopathic non-lupus FHN
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Orphanet_567544 |
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CATCH 22
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Orphanet_567 |
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DiGeorge sequence
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Orphanet_567 |
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DiGeorge syndrome
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Orphanet_567 |
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Microdeletion 22q11.2
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Orphanet_567 |
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Monosomy 22q11
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Orphanet_567 |
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Sedlackova syndrome
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Orphanet_567 |
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Shprintzen syndrome
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Orphanet_567 |
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Takao syndrome
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Orphanet_567 |
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Velocardiofacial syndrome
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Orphanet_567 |
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BILU syndrome
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Orphanet_567502 |
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