Pick one of the followings
*Some genes may be words of complete meaning. In any case, if present, they are relevant key words.
Legend:
*** | p-value <= 0.001 |
** | p-value <= 0.01 |
* | p-value <= 0.05 |
n.s. | not significant |
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Top Ranked Genes, Molecules or Short Names*
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Top Ranked Key Phrases
Progressive familial intrahepatic cholestasis pfic ***
Peripheral pulmonary artery stenosis ***
Progressive familial intrahepatic cholestasis ***
Autosomal dominant disorder characterized ***
End stage liver disease ***
Alagille syndrome arteriohepatic dysplasia ***
Peripheral pulmonary stenosis ***
Autosomal dominant disorder ***
Interlobular bile ducts ***
Intrahepatic bile ducts **
Alpha 1 antitrypsin deficiency **
Notch signaling pathway **
Cholestatic liver disease **
Congenital hepatic fibrosis **
Congenital heart disease **
Congenital heart defects **
Characteristic facial appearance *
Alagille syndrome patients *
Multisystem disorder n.s.
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Top Ranked Mesh Terms
Bile ducts intrahepatic ***
Retrospective studies ***
Cholestasis intrahepatic ***
Serrate-jagged proteins ***
Calcium-binding proteins ***
Intercellular signaling peptides and proteins ***
Liver transplantation ***
Chromosomes human pair 20 ***
Abnormalities multiple ***
Diagnosis differential ***
Heart defects congenital **
Dna mutational analysis **
In situ hybridization fluorescence **
Severity of illness index **
Tomography x-ray computed **
Gene expression regulation developmental **
Postoperative complications **
Carcinoma hepatocellular *
Magnetic resonance imaging *
Vascular surgical procedures *
Focal nodular hyperplasia *
Cardiac catheterization *
Exocrine pancreatic insufficiency *
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Top Ranked Mesh Terms (Symptoms)
Postoperative complications **
Neovascularization pathologic *
Intellectual disability *
Fetal growth retardation *
Alpha 1-antitrypsin deficiency n.s.
Constriction pathologic n.s.
Jaundice obstructive n.s.
Genetic predisposition to disease n.s.
Chromosome aberrations n.s.
Hernia diaphragmatic n.s.
Subarachnoid hemorrhage n.s.
Translocation genetic n.s.
Sex chromosome aberrations n.s.
Chromosome inversion n.s.
Pigmentation disorders n.s.
Chromosome fragility n.s.
Intraoperative complications n.s.
Hematoma epidural cranial n.s.
Intracranial hemorrhages n.s.
Graft occlusion vascular n.s.
Dilatation pathologic n.s.
Remission spontaneous n.s.
Hypertrophy right ventricular n.s.
Chromosome duplication n.s.
Hearing loss sensorineural n.s.
Disease susceptibility n.s.
Neoplasm recurrence local n.s.
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