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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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DA5D
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Orphanet_329457 |
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DYT25
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Orphanet_329466 |
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Non-DS-AMKL
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Orphanet_329469 |
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Hapnes-Boman-Skeie syndrome
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Orphanet_3294 |
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Dystonia 25
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Orphanet_329466 |
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Lipoprotein glomerulopathy
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Orphanet_329481 |
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Spastic paraplegia-Paget disease of bone syndrome
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Orphanet_329475 |
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Autosomal dominant focal dystonia, DYT25 type
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Orphanet_329466 |
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Acute megakaryoblastic leukemia in children without trisomy 21
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Orphanet_329469 |
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Adult-onset distal myopathy due to VCP mutation
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Orphanet_329478 |
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Extensor tendons of finger anomalies
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Orphanet_3294 |
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Distal arthrogryposis type 5 without ophthalmoparesis
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Orphanet_329457 |
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Distal arthrogryposis type 5 without ophthalmoplegia
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Orphanet_329457 |
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Distal arthrogryposis type 5D
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Orphanet_329457 |
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