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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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Segmental arterial mediolysis
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Orphanet_645350 |
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X-linked hereditary motor and sensory neuropathy
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Orphanet_64747 |
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Limited dorsal myeloschisis
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Orphanet_645196 |
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Dermatomyositis sine myositis
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Orphanet_645617 |
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Benign idiopathic neonatal seizures
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Orphanet_64545 |
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Benign nonfamilial neonatal seizures
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Orphanet_64545 |
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Current pressure-sensitive neuropathy
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Orphanet_640 |
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Multifocal motor neuropathy
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Orphanet_641 |
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Giant axonal neuropathy
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Orphanet_643 |
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Multifocal motor neuropathy with conduction block
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Orphanet_641 |
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Rare adrenocortical nodular disease
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Orphanet_649017 |
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Spina bifida occulta
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Orphanet_645202 |
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Polymorphic eruption of pregnancy
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Orphanet_64745 |
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Primary tuberculosis of the digestive system
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Orphanet_645859 |
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Idiopathic pregnancy-associated osteoporosis
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Orphanet_647823 |
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