Search on: ALAGILLE SYNDROME 
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Descriptor English:   Alagille Syndrome 
Descriptor Spanish:   Síndrome de Alagille 
Descriptor Portuguese:   Síndrome de Alagille 
Synonyms English:   Arteriohepatic Dysplasia
Dysplasia, Arteriohepatic  
Tree Number:   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
Definition English:   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). 
History Note English:   92 
Allowable Qualifiers English:  
blood cerebrospinal fluid
chemically induced classification
complications diet therapy
diagnosis drug therapy
economics ethnology
embryology enzymology
epidemiology etiology
genetics history
immunology metabolism
microbiology mortality
nursing pathology
prevention & control physiopathology
parasitology psychology
radiography rehabilitation
radionuclide imaging radiotherapy
surgery therapy
ultrastructure urine
ultrasonography veterinary
virology  
Record Number:   30271 
Unique Identifier:   D016738 

Occurrence in VHL:
 

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