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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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Alpha-1-antitrypsin deficiency
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Orphanet_60 |
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Alpha1-antitrypsin deficiency
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Orphanet_60 |
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Silver staining
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Orphanet_60014 |
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Catlin marks
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Orphanet_60015 |
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Pulmonary pseudolymphoma
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Orphanet_60026 |
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Loeys-Dietz syndrome
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Orphanet_60030 |
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Idiopathic bronchiectasis
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Orphanet_60033 |
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Alcock syndrome
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Orphanet_60039 |
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Pudendal algia
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Orphanet_60039 |
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Pudendal neuralgia
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Orphanet_60039 |
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Pudendal neuropathy
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Orphanet_60039 |
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Clark-Baraitser syndrome
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Orphanet_600731 |
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Legionella infection
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Orphanet_600832 |
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GNE myopathy
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Orphanet_602 |
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Nonaka myopathy
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Orphanet_602 |
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