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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.
Non-syndromic congenital functional defect of phagocytes
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Orphanet_674896 |
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Non-syndromic constitutional functional phagocyte defect
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Orphanet_674896 |
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Acquired elastotic haemangioma
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Orphanet_675597 |
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Eccrine angiomatous hamartoma
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Orphanet_673568 |
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Vegetant intravascular hemangioendothelioma
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Orphanet_673525 |
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Papillary capillary hemangioma
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Orphanet_673543 |
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Targetoid hemosiderotic hemangioma
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Orphanet_675362 |
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Large segmental hemangioma
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Orphanet_675380 |
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Littoral cell hemangioma of the spleen
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Orphanet_673538 |
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Pleural mesothelioma in situ
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Orphanet_675841 |
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Peritoneal mesothelioma in situ
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Orphanet_676036 |
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Isolated segmental infantile hemangioma
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Orphanet_675380 |
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Masson's vegetant intravascular hemangiendothelioma
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Orphanet_673525 |
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Autosomal dominant late-onset retinal degeneration
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Orphanet_67042 |
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Chronic lymphocytic leukemia
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Orphanet_67038 |
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