Alagille syndrome due to 20p12 microdeletion

MONDO:0016861

Also known as: Alagille syndrome due to del(20)(p12), Alagille syndrome due to monosomy 20p12, Alagille-Watson syndrome due to monosomy 20p12, Arteriohepatic dysplasia due to monosomy 20p12, syndromic bile duct paucity due to monosomy 20p12

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