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| created at |
2024-09-23 16:23:50 UTC |
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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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PFCP
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Orphanet_90042 |
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Familial erythrocytosis
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Orphanet_90042 |
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Primary familial and congenital polycythemia
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Orphanet_90042 |
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Congenital polycythemia due to erythropoietin receptor mutation
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Orphanet_90042 |
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Primary congenital erythrocytosis
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Orphanet_90042 |
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Primary familial polycythemia
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Orphanet_90042 |
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