"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.
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).
- Alagille Syndrome
- Syndrome, Alagille
- Dysplasia, Arteriohepatic
- Hepatic Ductular Hypoplasia, Syndromatic
- Hepatofacioneurocardiovertebral Syndrome
- Hepatofacioneurocardiovertebral Syndromes
- Syndrome, Hepatofacioneurocardiovertebral
- Syndromes, Hepatofacioneurocardiovertebral
- Watson Alagille Syndrome
- Syndrome, Watson Alagille
- Cardiovertebral Syndrome
- Cardiovertebral Syndromes
- Syndrome, Cardiovertebral
- Syndromes, Cardiovertebral
- Watson-Miller syndrome
- syndrome, Watson-Miller
- Alagille Watson Syndrome
- Alagille Watson Syndromes
- Syndrome, Alagille Watson
- Syndromes, Alagille Watson
- Alagille-Watson Syndrome
- Syndrome, Alagille-Watson
- Arteriohepatic Dysplasia
- Arteriohepatic Dysplasias
- Dysplasias, Arteriohepatic
- Cholestasis with Peripheral Pulmonary Stenosis
- Watson Miller Syndrome
- Syndrome, Watson Miller
Paucity of Interlobular Bile Ducts
- Paucity of Interlobular Bile Ducts
- Hepatic Ductular Hypoplasia
- Ductular Hypoplasia, Hepatic
- Ductular Hypoplasias, Hepatic
- Hepatic Ductular Hypoplasias
- Hypoplasia, Hepatic Ductular
- Hypoplasias, Hepatic Ductular
Below are MeSH descriptors whose meaning is more general than "Alagille Syndrome".
Below are MeSH descriptors whose meaning is more specific than "Alagille Syndrome".
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