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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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EOFAD
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Orphanet_1020 |
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Medullar disease
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Orphanet_102000 |
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Rare ataxia
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Orphanet_102002 |
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Neurovascular malformation
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Orphanet_102006 |
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Classic lissencephaly
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Orphanet_102009 |
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Pure HSP
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Orphanet_102012 |
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Pure SPG
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Orphanet_102012 |
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Uncomplicated HSP
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Orphanet_102012 |
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Uncomplicated SPG
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Orphanet_102012 |
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Complex HSP
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Orphanet_102013 |
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Complex SPG
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Orphanet_102013 |
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Complicated HSP
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Orphanet_102013 |
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Complicated SPG
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Orphanet_102013 |
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Autosomal deletion
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Orphanet_102020 |
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Autosomal monosomy
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Orphanet_102020 |
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