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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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Nevus of Ito
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Orphanet_263432 |
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Mesomelic dysplasia, Kozlowski-Reardon type
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Orphanet_2631 |
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Mesomelic dwarfism, Langer type
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Orphanet_2632 |
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Spondyloepimetaphyseal dysplasia, Maroteaux type
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Orphanet_263482 |
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Mesomelic dwarfism, Nievergelt type
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Orphanet_2633 |
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Mesomelic dysplasia, Nievergelt type
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Orphanet_2633 |
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Nevus of Ota
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Orphanet_263425 |
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Mesomelic dysplasia, Reardon type
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Orphanet_2631 |
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Mesomelic dwarfism, Reinhardt-Pfeiffer type
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Orphanet_2634 |
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Polysomy of X chromosome
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Orphanet_263723 |
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GSD type XV
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Orphanet_263297 |
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Glycogenosis type XV
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Orphanet_263297 |
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X and Y chromosomal anomaly
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Orphanet_263749 |
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Protein S acquired deficiency
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Orphanet_26349 |
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Nevus fuscocaeruleus acromiodeltoideus
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Orphanet_263432 |
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