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Alagille syndrome due to 20p12 microdeletion

Disease Export to PDF
Name:
Alagille syndrome due to 20p12 microdeletion
ORPHAcode:
261600
Synonyms:
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
XREF(s):
Orphanet
ICD-10
OMIM
Analyte(s):
JAG1
Created:
13 May 2019 - 01:02
Changed:
22 Jun 2023 - 16:14