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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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Lymphangioleiomyomatosis
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Orphanet_538 |
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XLP1
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Orphanet_538931 |
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XLP2
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Orphanet_538934 |
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ITK deficiency
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Orphanet_538963 |
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Familial multiple discoid fibromas
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Orphanet_538756 |
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X-linked lymphoproliferative disease due to SAP deficiency
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Orphanet_538931 |
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X-linked lymphoproliferative disease due to SH2D1A deficiency
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Orphanet_538931 |
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X-linked lymphoproliferative disease due to XIAP deficiency
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Orphanet_538934 |
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Combined immunodeficiency due to CD70 deficiency
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Orphanet_538958 |
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Combined immunodeficiency due to ITK deficiency
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Orphanet_538963 |
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Classic pyoderma gangrenosum
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Orphanet_538863 |
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Ulcerative pyoderma gangrenosum
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Orphanet_538863 |
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Pustular pyoderma gangrenosum
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Orphanet_538866 |
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Bullous pyoderma gangrenosum
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Orphanet_538869 |
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Phemphigoid pyoderma gangrenosum
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Orphanet_538869 |
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