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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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ALSP
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Orphanet_313808 |
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FPSG
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Orphanet_313808 |
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GPSC
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Orphanet_313808 |
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HDLS
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Orphanet_313808 |
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POLD
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Orphanet_313808 |
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Familial dementia, Neumann type
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Orphanet_313808 |
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Pigmentary orthochromatic leukodystrophy
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Orphanet_313808 |
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Hereditary diffuse leukoencephalopathy with spheroids
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Orphanet_313808 |
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Subcortical gliosis of Neumann
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Orphanet_313808 |
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Familial progressive subcortical gliosis
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Orphanet_313808 |
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