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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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Nasopharyngeal carcinoma
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Orphanet_150 |
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Adrenocortical carcinoma
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Orphanet_1501 |
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Sharma-Kapoor-Ramji syndrome
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Orphanet_1506 |
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COVESDEM syndrome
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Orphanet_1507 |
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Coxoauricular syndrome
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Orphanet_1508 |
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Coxopodopatellar syndrome
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Orphanet_1509 |
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Ischiopatellar dysplasia
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Orphanet_1509 |
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Scott-Taor syndrome
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Orphanet_1509 |
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Autosomal recessive Robinow syndrome
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Orphanet_1507 |
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Thin ribs-tubular bones-dysmorphism syndrome
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Orphanet_1506 |
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Squamous cell carcinoma of the nasopharynx
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Orphanet_150 |
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Costovertebral segmentation defect-mesomelia syndrome
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Orphanet_1507 |
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Short rib-polydactyly syndrome
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Orphanet_1505 |
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Small patella syndrome
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Orphanet_1509 |
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