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Ontology Browser
Term:
Parent Terms Term With Siblings Child Terms
immune system disease +     
liver disease +     
Pseudo-TORCH Syndrome +     
Abnormal Neutrophil Chemotactic Response 
Alcoholic Liver Diseases +   
allergic disease +   
alpha 1-antitrypsin deficiency  
alveolar echinococcosis  
autoimmune disease +   
Budd-Chiari syndrome +   
capillariasis 
Carnitine Palmitoyltransferase II Deficiency, Infantile  
Chondroitin-6-Sulfaturia, Defective Cellular Immunity, Nephrotic Syndrome 
clonorchiasis  
COACH syndrome +   
Cyanosis and Hepatic Disease 
cystic echinococcosis  
Focal Nodular Hyperplasia  
Glycogen Storage Disease 0, Liver  
glycogen storage disease IX +   
glycogen storage disease VI  
graft-versus-host disease +   
Growth Hormone Insensitivity with Immune Dysregulation +   
GROWTH RETARDATION, INTELLECTUAL DEVELOPMENTAL DISORDER, HYPOTONIA, AND HEPATOPATHY  
GSD IV, Nonprogressive Hepatic 
hemolytic disease of the fetus +   
Hepatic Granuloma 
Hepatic Insufficiency +   
Hepatic Porphyrias +   
hepatic tuberculosis 
hepatic vascular disease +   
hepatitis +   
Hepatomegaly +   
hepatopulmonary syndrome  
hepatorenal syndrome  
hypersensitivity reaction disease +   
IMAGEI Syndrome  
Immune Reconstitution Inflammatory Syndrome 
Immune Suppression 
immune system cancer +   
immunoglobulin light chain amyloidosis  
Immunoproliferative Disorders +   
Immunoskeletal Dysplasia with Neurodevelopmental Abnormalities  
INFLAMMATORY BOWEL DISEASE, IMMUNODEFICIENCY, AND ENCEPHALOPATHY  
Inhibition of Lymphoblastic Transformation 
INTERSTITIAL LUNG AND LIVER DISEASE  
intrahepatic cholestasis +   
Liver Abscess +   
liver cirrhosis +   
Liver Fibrocystic Disease and Polydactyly 
liver inflammatory pseudotumor 
Liver Injury +   
Liver Neoplasms +   
lymphatic system disease +   
membranoproliferative glomerulonephritis +   
mitochondrial DNA depletion syndrome 6  
Monocyte Chemotactic Disorder 
opisthorchiasis  
paragonimiasis 
Parasitic Liver Diseases +   
Phosphoenolpyruvate Carboxykinase Deficiency +   
polycystic echinococcosis 
polycystic liver disease +   
primary immunodeficiency disease +   
pseudo-TORCH syndrome 1  
Pseudo-TORCH Syndrome 2  
An autosomal recessive multisystem disorder characterized by antenatal onset of intracranial hemorrhage, calcification, brain malformations, liver dysfunction, and often thrombocytopenia. The disorder results from inappropriate activation of the interferon (IFN) immunologic pathway.
Pseudo-TORCH Syndrome 3  
Radiation Sensitivity of Natural Killer Activity 
Recurrent Infections, with Encephalopathy, Hepatic Dysfunction, and Cardiovascular Malformations  
renal-hepatic-pancreatic dysplasia +   
Retinohepatoendocrinologic Syndrome 
serum amyloid A amyloidosis 
Severe Congenital Liver Disease  
steatotic liver disease +   
Thrombocytopenic Purpura +   
toxocariasis +   
Transfusion Reaction +   
Transplant Rejection +   
Trichohepatoneurodevelopmental Syndrome  
tyrosinemia type II  
visceral leishmaniasis  
Wilson disease +   
Zellweger syndrome +   

Synonyms
Exact Synonyms: PTORCH2 ;   USP18-RELATED CONDITION
Primary IDs: MIM:617397
Definition Sources: MIM:617397

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