Autosomal dominant hereditary disorder
Biliary tract dysplasia
Congenital anomaly of biliary tract
Congenital anomaly of liver
Developmental hereditary disorder
Digestive system hereditary disorder
Hereditary cancer-predisposing syndrome
Lesion of liver
Multiple system malformation syndrome
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Arteriohepatic dysplasia (disorder)
Arteriohepatic dysplasia
Watson-Alagille syndrome
Alagille syndrome
Id31742004
StatusPrimitive
Associated morphologyDysplasia
Finding siteIntrahepatic biliary tract structure
OccurrenceCongenital
Pathological processPathological developmental process
Global Patient Set
SNOMED CT to Orphanet simple map
RIVM authorized national diagnosis thesaurus to ICD10 complex mapping reference set
TargetQ44.7
TermOverige congenitale misvormingen van lever
SNOMED CT to ICD-10 extended map
TargetQ44.7
RuleTRUE
AdviceALWAYS Q44.7
CorrelationSNOMED CT source code to target map code correlation not specified