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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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Congenital trismus
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Orphanet_210576 |
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Hall-Riggs syndrome
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Orphanet_2107 |
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Hallermann-Streiff syndrome
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Orphanet_2108 |
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Oculomandibulofacial syndrome
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Orphanet_2108 |
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Dennis-Fairhurst-Moore syndrome
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Orphanet_2109 |
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Hallermann-Streiff-like syndrome
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Orphanet_2109 |
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GTP cyclohydrolase I deficiency
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Orphanet_2102 |
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Temporomandibular joint anomaly
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Orphanet_210581 |
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Interleukin-1 receptor antagonist deficiency
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Orphanet_210115 |
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Congenital alveolar capillary dysplasia
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Orphanet_210122 |
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Adult hepatocellular carcinoma
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Orphanet_210159 |
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Sickness of disembarkment
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Orphanet_210272 |
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Mal de débarquement
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Orphanet_210272 |
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Spindle cell hemangioendothelioma
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Orphanet_210584 |
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Spindle cell hemangioma
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Orphanet_210584 |
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