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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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SPG36
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Orphanet_320365 |
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SPG41
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Orphanet_320355 |
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SPG43
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Orphanet_320370 |
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SPG45
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Orphanet_320396 |
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SPG46
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Orphanet_320391 |
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SPG49
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Orphanet_320385 |
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SPG54
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Orphanet_320380 |
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SPG55
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Orphanet_320375 |
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SPG65
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Orphanet_320396 |
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Maternally-inherited SPG
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Orphanet_320360 |
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Pure or complex X-linked spastic paraplegia
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Orphanet_320350 |
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Pure or complex autosomal dominant spastic paraplegia
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Orphanet_320342 |
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Pure or complex autosomal recessive spastic paraplegia
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Orphanet_320346 |
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Pure or complex familial spastic paraplegia
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Orphanet_320335 |
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Pure or complex hereditary spastic paraplegia
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Orphanet_320335 |
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