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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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Progressive myoclonus epilepsy
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Orphanet_98261 |
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Macrophage or histiocytic tumor
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Orphanet_98288 |
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Acute myeloid leukemia with recurrent genetic anomaly
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Orphanet_98277 |
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Genetic non-syndromic obesity
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Orphanet_98267 |
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Congenital absence of the pulmonary valve
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Orphanet_982 |
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AML with recurrent genetic anomaly
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Orphanet_98277 |
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Neonatal epilepsy syndrome
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Orphanet_98257 |
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Infantile epilepsy syndrome
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Orphanet_98258 |
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Childhood-onset epilepsy syndrome
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Orphanet_98259 |
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Adolescent-onset epilepsy syndrome
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Orphanet_98260 |
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Plasma cell tumor
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Orphanet_98282 |
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Dendritic cell tumor
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Orphanet_98289 |
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Absent pulmonary valve syndrome
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Orphanet_982 |
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