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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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FPD/AML
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Orphanet_71290 |
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FPDMM
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Orphanet_71290 |
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FPS/AML
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Orphanet_71290 |
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NMOSD
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Orphanet_71211 |
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Autoimmune thrombocytopenia
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Orphanet_71203 |
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Devic disease
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Orphanet_71211 |
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SCHAD deficiency
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Orphanet_71212 |
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Sandifer syndrome
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Orphanet_71272 |
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Rh-null syndrome
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Orphanet_71275 |
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Classic GLUT1-DS
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Orphanet_71277 |
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CANDA syndrome
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Orphanet_71279 |
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CANOMAD syndrome
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Orphanet_71279 |
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ATRUS syndrome
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Orphanet_71289 |
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Inherited GS deficiency
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Orphanet_71278 |
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Classic GLUT1 deficiency syndrome
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Orphanet_71277 |
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