| D007231 |
Infant, Newborn |
An infant during the first 28 days after birth. |
Neonate,Newborns,Infants, Newborn,Neonates,Newborn,Newborn Infant,Newborn Infants |
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| D008099 |
Liver |
A large lobed glandular organ in the abdomen of vertebrates that is responsible for detoxification, metabolism, synthesis and storage of various substances. |
Livers |
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| D008107 |
Liver Diseases |
Pathological processes of the LIVER. |
Liver Dysfunction,Disease, Liver,Diseases, Liver,Dysfunction, Liver,Dysfunctions, Liver,Liver Disease,Liver Dysfunctions |
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| D002779 |
Cholestasis |
Impairment of bile flow due to obstruction in small bile ducts (INTRAHEPATIC CHOLESTASIS) or obstruction in large bile ducts (EXTRAHEPATIC CHOLESTASIS). |
Bile Duct Obstruction,Biliary Stasis,Bile Duct Obstructions,Biliary Stases,Cholestases,Duct Obstruction, Bile,Duct Obstructions, Bile,Obstruction, Bile Duct,Obstructions, Bile Duct,Stases, Biliary,Stasis, Biliary |
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| D006801 |
Humans |
Members of the species Homo sapiens. |
Homo sapiens,Man (Taxonomy),Human,Man, Modern,Modern Man |
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| D001653 |
Bile Ducts, Intrahepatic |
Passages within the liver for the conveyance of bile. Includes right and left hepatic ducts even though these may join outside the liver to form the common hepatic duct. |
Bile Duct, Intrahepatic,Duct, Intrahepatic Bile,Ducts, Intrahepatic Bile,Intrahepatic Bile Duct,Intrahepatic Bile Ducts |
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| D001656 |
Biliary Atresia |
Progressive destruction or the absence of all or part of the extrahepatic BILE DUCTS, resulting in the complete obstruction of BILE flow. Usually, biliary atresia is found in infants and accounts for one third of the neonatal cholestatic JAUNDICE. |
Atresia, Biliary,Biliary Atresia, Extrahepatic,Biliary Atresia, Intrahepatic,Extrahepatic Biliary Atresia,Familial Extrahepatic Biliary Atresia,Idiopathic Extrahepatic Biliary Atresia,Intrahepatic Biliary Atresia,Atresia, Extrahepatic Biliary,Atresia, Intrahepatic Biliary |
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| D001706 |
Biopsy |
Removal and pathologic examination of specimens from the living body. |
Biopsies |
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| D016738 |
Alagille Syndrome |
A multisystem disorder that is characterized by aplasia of intrahepatic bile ducts (BILE DUCTS, INTRAHEPATIC), and malformations in the cardiovascular system, the eyes, the vertebral column, and the facies. Major clinical features include JAUNDICE, and congenital heart disease with peripheral PULMONARY STENOSIS. Alagille syndrome may result from heterogeneous gene mutations, including mutations in JAG1 on CHROMOSOME 20 (Type 1) and NOTCH2 on CHROMOSOME 1 (Type 2). |
Arteriohepatic Dysplasia,Dysplasia, Arteriohepatic,Alagille Syndrome 1,Alagille Syndrome 2,Alagille Watson Syndrome,Alagille's Syndrome,Alagille-Watson Syndrome,Arteriohepatic Dysplasia (AHD),Cardiovertebral Syndrome,Cholestasis with Peripheral Pulmonary Stenosis,Hepatic Ductular Hypoplasia,Hepatic Ductular Hypoplasia, Syndromatic,Hepatofacioneurocardiovertebral Syndrome,Paucity of Interlobular Bile Ducts,Watson Alagille Syndrome,Watson Miller Syndrome,Watson-Miller syndrome,Alagilles Syndrome,Ductular Hypoplasia, Hepatic,Dysplasia, Arteriohepatic (AHD),Hypoplasia, Hepatic Ductular,Syndrome, Alagille,Syndrome, Alagille Watson,Syndrome, Alagille's,Syndrome, Alagille-Watson,Syndrome, Cardiovertebral,Syndrome, Hepatofacioneurocardiovertebral,Syndrome, Watson Alagille,Syndrome, Watson Miller,syndrome, Watson-Miller |
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