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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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CIL-F
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Orphanet_583097 |
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MPS6
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Orphanet_583 |
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MPSVI
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Orphanet_583 |
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ARSB deficiency
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Orphanet_583 |
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ASB deficiency
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Orphanet_583 |
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Maroteaux-Lamy disease
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Orphanet_583 |
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Mucopolysaccharidosis type 6
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Orphanet_583 |
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Mucopolysaccharidosis type VI
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Orphanet_583 |
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Arylsulfatase B deficiency
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Orphanet_583 |
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N-acetylgalactosamine 4-sulfatase deficiency
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Orphanet_583 |
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Phosphoserine aminotransferase deficiency, prenatal form
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Orphanet_583602 |
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3-phosphoglycerate dehydrogenase deficiency, prenatal form
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Orphanet_583607 |
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3-phosphoserine phosphatase deficiency, prenatal form
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Orphanet_583612 |
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Facial infused lipomatosis
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Orphanet_583097 |
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Fibroadipose infiltrating lipomatosis
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Orphanet_583097 |
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