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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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Del(9)(p13)
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Orphanet_324313 |
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HIBM4
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Orphanet_324381 |
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Sweet syndrome
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Orphanet_3243 |
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Monosomy 9p13
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Orphanet_324313 |
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Congenital achiasma
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Orphanet_324353 |
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Hereditary inclusion body myopathy type 4
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Orphanet_324381 |
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Acute febrile neutrophilic dermatosis
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Orphanet_3243 |
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Sinoatrial node dysfunction and deafness
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Orphanet_324321 |
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Sinoatrial node dysfunction and hearing loss
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Orphanet_324321 |
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9p13 microdeletion syndrome
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Orphanet_324313 |
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