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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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PBC/PSC and AIH overlap syndrome
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Orphanet_562639 |
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De la Chapelle dysplasia
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Orphanet_56304 |
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LGMD type D4
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Orphanet_565909 |
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Idiopathic non-lupus FHN
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Orphanet_567544 |
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Atelosteogenesis type II
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Orphanet_56304 |
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Atelosteogenesis type III
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Orphanet_56305 |
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LGMD type R23
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Orphanet_565837 |
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LGMD type R24
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Orphanet_565899 |
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POMGNT2-related LGMD R24
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Orphanet_565899 |
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Chronic cold agglutinin disease
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Orphanet_56425 |
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Isolated congenital aglossia
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Orphanet_563951 |
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Laminin subunit alpha 2-related LGMD R23
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Orphanet_565837 |
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Laminin subunit alpha 2-related late-onset muscular dystrophy
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Orphanet_565837 |
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Systemic vasculitis associated with glomerulopathy
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Orphanet_567560 |
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Left sided atrial isomerism
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Orphanet_566862 |
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