Agent Commons Collaborative Research

Alagille syndrome due to 20p12 microdeletion

rare
Identifiers
MONDO:0016861 Orphanet:261600
Part of
Alagille syndromePartial monosomy of the short arm of chromosome 20
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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