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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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HCL-C
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Orphanet_58017 |
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ITPN
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Orphanet_580572 |
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MPS2
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Orphanet_580 |
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MPSII
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Orphanet_580 |
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Osteoblastoma
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Orphanet_58040 |
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Hunter syndrome
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Orphanet_580 |
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Leukemic reticuloendotheliosis
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Orphanet_58017 |
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Mucopolysaccharidosis type 2
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Orphanet_580 |
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Mucopolysaccharidosis type II
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Orphanet_580 |
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Lethal brain and heart developmental defects
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Orphanet_580933 |
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Classic hairy cell leukemia
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Orphanet_58017 |
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Punctate inner choroidopathy
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Orphanet_580951 |
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Iduronate 2-sulfatase deficiency
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Orphanet_580 |
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QRICH1-related intellectual disability-chondrodysplasia syndrome
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Orphanet_580940 |
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Intraductal tubulopapillary neoplasm of pancreas
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Orphanet_580572 |
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