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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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Hurler-Scheie syndrome
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Orphanet_93476 |
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Achondroplasia-SCID syndrome
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Orphanet_935 |
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Glomerular disease
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Orphanet_93548 |
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AApoAI amyloidosis
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Orphanet_93560 |
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ALys amyloidosis
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Orphanet_93561 |
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Lysozyme amyloidosis
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Orphanet_93561 |
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AFib amyloidosis
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Orphanet_93562 |
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Juvenile PM
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Orphanet_93568 |
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Juvenile polymyositis
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Orphanet_93568 |
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Thrombotic microangiopathy
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Orphanet_93573 |
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Congenital TTP
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Orphanet_93583 |
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Familial TTP
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Orphanet_93583 |
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Upshaw-Schulman syndrome
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Orphanet_93583 |
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Acquired TTP
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Orphanet_93585 |
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Late-onset nephronophthisis
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Orphanet_93589 |
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