OMOP Concept 4151863
Congenital abnormality of liver and/or biliary tract
StandardConditionSNOMED268213006Disorder
Maps from
20
Descendants
109
Valid from
31 Jan 2002
Valid to
31 Dec 2099
OMOP concepts
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Source codes that map to this concept
20 source codes normalize to Congenital abnormality of liver and/or biliary tract via the OMOP "Maps to" relationship.
Synonyms
Alternative names recorded for Congenital abnormality of liver and/or biliary tract across source vocabularies.
- anomalía congénita de hígado y/o tracto biliar
- anomalía congénita de hígado y/o vía biliar
- anomalía congénita de hígado y/o vía biliar (trastorno)
- Congenital abnormality of liver and/or biliary tract (disorder)
- Liver and biliary system anomalies
Where it sits in the hierarchy
Ordered by distance - 1 is a direct parent or child.
Broader concepts
(24)Roll up to these when you need a wider cohort.
- 1Congenital anomaly of abdomen
- 1Congenital anomaly of digestive organ
- 1Disorder of liver and/or biliary tract
- 2Congenital anomaly of digestive system
- 2Congenital anomaly of lower trunk
- 2Disorder of abdomen
- 2Disorder of digestive organ
- 3Congenital abnormality of lower limb and pelvic girdle
- 3Congenital anomaly of trunk
- 3Congenital malformation
- 3Disorder of abdominopelvic segment of trunk
- 3Disorder of digestive system
- 3Disorder of digestive system specific to fetus OR newborn
- 3Finding of abdomen
- 4Congenital disease
- 4Developmental disorder
- 4Digestive system finding
- 4Disorder of body system
- 4Disorder of fetus and/or newborn
- 4Disorder of trunk
- 4Finding of abdominopelvic segment of trunk
- 5Clinical finding
- 5Disease
- 5Finding of trunk structure
Narrower concepts
(109)Included automatically when you query with descendants.
- 1Congenital absence of liver and/or gallbladder
- 1Congenital anomaly of biliary tract
- 1Congenital anomaly of liver
- 1Liver and/or biliary duplication
- 2Abnormal liver lobulation
- 2Accessory liver
- 2Arteriohepatic dysplasia
- 2Arteriovenous malformation of liver
- 2Autosomal dominant polycystic liver disease
- 2Biliary anomalies
- 2Cholestasis with pigmentary retinopathy and cleft palate syndrome
- 2Congenital abnormal fusion of liver lobes
- 2Congenital abnormality of hepatic vein
- 2Congenital abnormal shape of liver
- 2Congenital absence of liver
- 2Congenital anomaly of bile ducts
- 2Congenital anomaly of gallbladder
- 2Congenital choledochal cyst
- 2Congenital cholestatic syndrome
- 2Congenital dilatation of lobar intrahepatic bile duct
- 2Congenital dilatation of lobar intrahepatic bile duct with obstruction
- 2Congenital duplication of biliary duct
- 2Congenital duplication of gallbladder
- 2Congenital duplication of liver
- 2Congenital hepatic fibrosis
- 2Congenital hepatomegaly
- 2Congenital hyperplasia of intrahepatic bile duct
- 2Congenital malposition of liver
- 2Congenital microhepatia
- 2Congenital paucity of intrahepatic bile ducts
- 2Congenital respiratory biliary fistula
- 2Dubin-Johnson syndrome
- 2Ectopic liver
- 2Focal nodular hypoplasia of liver
- 2Glycogenosis with glucoaminophosphaturia
- 2Intrahepatic biliary atresia
- 2Intrahepatic biliary hypoplasia
- 2Liver hyperplasia
- 2Microhepatia
- 2Neonatal sclerosing cholangitis, ichthyosis, hypotrichosis syndrome
- 2Renal hepatic pancreatic dysplasia
- 2Trilobular liver
- 3Abnormal connection of hepatic vein to atrium
- 3Accessory hepatic duct
- 3Agenesis of liver
- 3Anomalous pulmonary venous drainage to hepatic veins
- 3Boichis syndrome
- 3Caroli disease
- 3Caroli syndrome
- 3Congenital abnormal long growth of bile duct
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