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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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Kjer optic atrophy
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Orphanet_98673 |
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Essential iris atrophy
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Orphanet_98981 |
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Spinal muscular atrophy with respiratory distress type 1
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Orphanet_98920 |
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Multiple system atrophy, parkinsonian type
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Orphanet_98933 |
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Autosomal recessive axonal CMT4C1
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Orphanet_98856 |
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Acute motor-sensory axonal GBS
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Orphanet_98917 |
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Acute motor-sensory axonal Guillain-Barré syndrome
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Orphanet_98917 |
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Acute motor axonal neuropathy
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Orphanet_98918 |
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Syndromic orbital border hypoplasia
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Orphanet_98606 |
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Rare digestive cancer
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Orphanet_98059 |
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Rare respiratory cancer
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Orphanet_98060 |
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Rare ORL cancer
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Orphanet_98061 |
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Rare gynaecological cancer
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Orphanet_98063 |
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Syndromic outer canthal malposition
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Orphanet_98576 |
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Rare allergic disease
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Orphanet_98050 |
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