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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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Full neurofibromatosis type 3
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Orphanet_93921 |
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Laryngo-tracheo-esophageal cleft type 3
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Orphanet_93940 |
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Laryngotracheoesophageal cleft type 3
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Orphanet_93940 |
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Polyepiphyseal dysplasia type 4
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Orphanet_93307 |
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Preaxial polydactyly type 4
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Orphanet_93338 |
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Laryngo-tracheo-esophageal cleft type 4
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Orphanet_93941 |
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Laryngotracheoesophageal cleft type 4
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Orphanet_93941 |
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Polyepiphyseal dysplasia type 5
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Orphanet_93311 |
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Postaxial polydactyly type A
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Orphanet_93334 |
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Postaxial polydactyly type B
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Orphanet_93335 |
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Mixed cryoglobulinemia type II
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Orphanet_93554 |
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Mixed cryoglobulinemia type III
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Orphanet_93555 |
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Bartter syndrome type III
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Orphanet_93605 |
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Renal agenesis, unilateral
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Orphanet_93100 |
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Kidney dysplasia, unilateral
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Orphanet_93172 |
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