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Alagillov syndróm
Č. záznamu d016738 Dátum 06.06.2025 Typ M - MESH Tematický termín Alagillov syndróm Iný termín Angličtina (Pseudonym) Arteriohepatic Dysplasia
Angličtina (Pseudonym) Dysplasia, Arteriohepatic
Slovenčina (Pseudonym) Alagilleho syndróm
Slovenčina (Pseudonym) Alagilleov syndróm
Slovenčina (Pseudonym) dysplázia hepatálnych artérií
Slovenčina (Pseudonym) dysplázia artériohepatálna
MDT C06.130.120.135.250.125C06.552.150.125C14.240.400.044C16.131.077.065C16.131.240.400.044C16.320.051 Poznámka 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). predmetové heslo
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