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Alagille Syndrome

"Alagille Syndrome" is a descriptor in the National Library of Medicine's controlled vocabulary thesaurus, MeSH (Medical Subject Headings). Descriptors are arranged in a hierarchical structure, which enables searching at various levels of specificity.

MeSH information

Definition

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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).

Descriptor ID	D016738
MeSH Number(s)	C06.130.120.135.250.125 C06.552.150.125 C14.240.400.044 C16.131.077.065 C16.131.240.400.044 C16.320.051
Concept/Terms	Alagille Syndrome Alagille Syndrome Syndrome, Alagille Alagille's Syndrome Alagilles Syndrome Syndrome, Alagille's Alagille-Watson Syndrome Syndrome, Alagille-Watson Arteriohepatic Dysplasia Cardiovertebral Syndrome Syndrome, Cardiovertebral Arteriohepatic Dysplasia (AHD) Dysplasia, Arteriohepatic (AHD) Dysplasia, Arteriohepatic Hepatic Ductular Hypoplasia, Syndromatic Hepatofacioneurocardiovertebral Syndrome Syndrome, Hepatofacioneurocardiovertebral Watson Alagille Syndrome Syndrome, Watson Alagille Watson Miller Syndrome Syndrome, Watson Miller Watson-Miller syndrome syndrome, Watson-Miller Alagille Watson Syndrome Syndrome, Alagille Watson Cholestasis with Peripheral Pulmonary Stenosis Alagille Syndrome 2 Alagille Syndrome 2 Paucity of Interlobular Bile Ducts Paucity of Interlobular Bile Ducts Hepatic Ductular Hypoplasia Ductular Hypoplasia, Hepatic Hypoplasia, Hepatic Ductular Alagille Syndrome 1 Alagille Syndrome 1

Below are MeSH descriptors whose meaning is more general than "Alagille Syndrome".

Diseases [C]
Digestive System Diseases [C06]
Biliary Tract Diseases [C06.130]
Bile Duct Diseases [C06.130.120]
Cholestasis [C06.130.120.135]
Cholestasis, Intrahepatic [C06.130.120.135.250]
Alagille Syndrome [C06.130.120.135.250.125]
Liver Diseases [C06.552]
Cholestasis, Intrahepatic [C06.552.150]
Alagille Syndrome [C06.552.150.125]
Cardiovascular Diseases [C14]
Cardiovascular Abnormalities [C14.240]
Heart Defects, Congenital [C14.240.400]
Alagille Syndrome [C14.240.400.044]
Congenital, Hereditary, and Neonatal Diseases and Abnormalities [C16]
Congenital Abnormalities [C16.131]
Abnormalities, Multiple [C16.131.077]
Alagille Syndrome [C16.131.077.065]
Cardiovascular Abnormalities [C16.131.240]
Heart Defects, Congenital [C16.131.240.400]
Alagille Syndrome [C16.131.240.400.044]
Genetic Diseases, Inborn [C16.320]
Alagille Syndrome [C16.320.051]

Below are MeSH descriptors whose meaning is related to "Alagille Syndrome".

Below are MeSH descriptors whose meaning is more specific than "Alagille Syndrome".

Publications

Timeline | Most Recent

This graph shows the total number of publications written about "Alagille Syndrome" by people in this website by year, and whether "Alagille Syndrome" was a major or minor topic of these publications.

Bar chart showing 3 publications over 3 distinct years, with a maximum of 1 publications in 2018 and 2019 and 2021

To see the data from this visualization as text, click here.

Year	Major Topic	Minor Topic	Total
2018	1	0	1
2019	0	1	1
2021	0	1	1

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Alagille Syndrome