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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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Acute sensory ataxic neuropathy
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Orphanet_231466 |
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Acquired HbH disease
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Orphanet_231401 |
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Autosomal dominant hyper-IgE syndrome due to STAT3 deficiency
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Orphanet_2314 |
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Acute panautonomic neuropathy
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Orphanet_231457 |
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Regional variant of GBS
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Orphanet_231416 |
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Functional variant of GBS
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Orphanet_231419 |
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PCB variant of GBS
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Orphanet_231426 |
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Pharyngo-cervico-brachial variant of GBS
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Orphanet_231426 |
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Paraparetic variant of GBS
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Orphanet_231445 |
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Regional variant of Guillain-Barré syndrome
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Orphanet_231416 |
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Functional variant of Guillain-Barré syndrome
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Orphanet_231419 |
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PCB variant of Guillain-Barré syndrome
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Orphanet_231426 |
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Pharyngeal-cervical-brachial variant of Guillain-Barré syndrome
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Orphanet_231426 |
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Pharyngo-cervico-brachial variant of Guillain-Barré syndrome
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Orphanet_231426 |
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Paraparetic variant of Guillain-Barré syndrome
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Orphanet_231445 |
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