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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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MIHF
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Orphanet_93926 |
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MIHV
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Orphanet_93926 |
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Syntelencephaly
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Orphanet_93926 |
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MIH type HPE
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Orphanet_93926 |
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Middle interhemispheric fusion variant
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Orphanet_93926 |
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Middle interhemispheric variant of holoprosencephaly
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Orphanet_93926 |
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Midline interhemispheric variant of holoprosencephaly
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Orphanet_93926 |
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