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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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Genetic HLH
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Orphanet_158038 |
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Primary HLH
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Orphanet_158038 |
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Distal deletion 10p
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Orphanet_1580 |
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Distal monosomy 10p
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Orphanet_1580 |
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Telomeric deletion 10p
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Orphanet_1580 |
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Hemophagocytic syndrome associated with an infection
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Orphanet_158048 |
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Indeterminate dendritic cell neoplasm
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Orphanet_158019 |
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Indeterminate dendritic cell tumor
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Orphanet_158019 |
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Indeterminate cell histiocytosis
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Orphanet_158019 |
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Progressive nodular histiocytosis
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Orphanet_158022 |
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Genetic hemophagocytic lymphohistiocytosis
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Orphanet_158038 |
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Primary hemophagocytic lymphohistiocytosis
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Orphanet_158038 |
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Acquired hemophagocytic lymphohistiocytosis
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Orphanet_158041 |
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Secondary hemophagocytic lymphohistiocytosis
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Orphanet_158041 |
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Hereditary progressive mucinous histiocytosis
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Orphanet_158025 |
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