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| created at |
2024-09-23 16:23:50 UTC |
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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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EPM7
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Orphanet_435438 |
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MEAK
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Orphanet_435438 |
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PME type 7
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Orphanet_435438 |
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Myoclonus epilepsy and ataxia due to potassium channel mutation
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Orphanet_435438 |
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Progressive myoclonic epilepsy due to KV3.1 deficiency
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Orphanet_435438 |
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Progressive myoclonic epilepsy type 7
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Orphanet_435438 |
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Progressive myoclonus epilepsy type 7
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Orphanet_435438 |
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