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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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Benign focal amyotrophy
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Orphanet_65684 |
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Breast implant-associated anaplastic large cell lymphoma
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Orphanet_667662 |
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Hereditary sensory and autonomic neuropathy type 4
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Orphanet_642 |
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Hereditary sensory and autonomic neuropathy type 5
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Orphanet_64752 |
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Hereditary sensory and autonomic neuropathy type IV
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Orphanet_642 |
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Hereditary sensory and autonomic neuropathy type V
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Orphanet_64752 |
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Non-syndromic sagittal and bilateral coronal synostosis
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Orphanet_620205 |
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Primary bone and joint tuberculosis
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Orphanet_645822 |
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Isolated bicoronal and metopic craniosynostosis
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Orphanet_620198 |
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Non-syndromic bicoronal and metopic craniosynostosis
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Orphanet_620198 |
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Painful legs and moving toes syndrome
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Orphanet_617440 |
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Pure hair and nail ectodermal dysplasia
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Orphanet_69084 |
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Vocal cord and pharyngeal distal myopathy
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Orphanet_600 |
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Isolated unicoronal and sagittal craniosynostosis
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Orphanet_620186 |
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Non-syndromic unicoronal and sagittal craniosynostosis
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Orphanet_620186 |
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