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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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Autosomal dominant spastic paraplegia type 10
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Orphanet_100991 |
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Autosomal dominant spastic paraplegia type 12
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Orphanet_100993 |
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Autosomal dominant spastic paraplegia type 13
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Orphanet_100994 |
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Autosomal recessive spastic paraplegia type 14
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Orphanet_100995 |
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Autosomal recessive spastic paraplegia type 15
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Orphanet_100996 |
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Autosomal dominant spastic paraplegia type 17
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Orphanet_100998 |
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Autosomal dominant spastic paraplegia type 19
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Orphanet_100999 |
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Autosomal dominant spastic paraplegia type 3
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Orphanet_100984 |
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Autosomal dominant spastic paraplegia type 3A
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Orphanet_100984 |
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Autosomal dominant spastic paraplegia type 4
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Orphanet_100985 |
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Autosomal recessive spastic paraplegia type 5A
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Orphanet_100986 |
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Autosomal dominant spastic paraplegia type 6
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Orphanet_100988 |
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Autosomal dominant spastic paraplegia type 8
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Orphanet_100989 |
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NET of stomach
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Orphanet_100075 |
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Neurogenic costoclavicular syndrome
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Orphanet_100073 |
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