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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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Syndromic bile duct paucity due to monosomy 20p12
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Orphanet_261600 |
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Alagille syndrome due to 20p12 microdeletion
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Orphanet_261600 |
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Alagille syndrome due to del(20)(p12)
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Orphanet_261600 |
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Alagille syndrome due to monosomy 20p12
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Orphanet_261600 |
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Alagille-Watson syndrome due to monosomy 20p12
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Orphanet_261600 |
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Arteriohepatic dysplasia due to monosomy 20p12
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Orphanet_261600 |
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