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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Broader categories

Cardiovascular disorder (1051) Disease (680) Heart disorder (300) Hereditary disease (176) Digestive system disorder (160) Eye disorder (102) Syndromic disease (25) Biliary tract disorder (19) Alagille syndrome (15) Human disease (14)

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