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

0 clinical trials for this condition and its sub-types, 0 tagged with Alagille syndrome due to 20p12 microdeletion itself.

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↑ Alagille syndrome (15) ↑ Partial monosomy of the short arm of chromosome 20 (0)

Including sub-types (0) Tagged with Alagille syndrome due to 20p12 microdeletion (0)

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