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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 Volkmann ischemic contracture syndrome
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Orphanet_641829 |
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Neonatal Volkmann ischemic contracture syndrome
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Orphanet_641829 |
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Multifocal motor neuropathy
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Orphanet_641 |
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Multifocal motor neuropathy with conduction block
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Orphanet_641 |
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Very early-onset schizophrenia
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Orphanet_641496 |
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Endogenous Cushing syndrome
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Orphanet_641613 |
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Neonatal compartment syndrome
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Orphanet_641829 |
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Central nervous system tuberculosis
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Orphanet_641396 |
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AR-HIES due to ZNF341 deficiency
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Orphanet_641368 |
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B-lymphoblastic leukemia/lymphoma with t(17;19)
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Orphanet_641375 |
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B-lymphoblastic leukemia/lymphoma with t(7;9)(q11.2;p13.2)
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Orphanet_641372 |
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