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Ontology Browser

Term:
Pseudo-TORCH Syndrome 2 (DOID:9001536)
Annotations: Rat: (1) Mouse: (1) Human: (1) Chinchilla: (1) Bonobo: (1) Dog: (1) Squirrel: (1) Pig: (1)
Parent Terms Term With Siblings Child Terms
liver disease +     
Abnormal Neutrophil Chemotactic Response 
Alcoholic Liver Diseases +   
alpha 1-antitrypsin deficiency  
alveolar echinococcosis  
Autoimmune Diseases +   
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  
fatty liver disease +   
fetal erythroblastosis +   
Focal Nodular Hyperplasia 
Glycogen Storage Disease 0, Liver  
glycogen storage disease VI  
Graft vs Host Disease  
GROWTH RETARDATION, INTELLECTUAL DEVELOPMENTAL DISORDER, HYPOTONIA, AND HEPATOPATHY  
GSD IV, Nonprogressive Hepatic 
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 Response to Synthetic Polypeptide--IrGAT 
Immune Suppression 
immune system cancer +   
Immunoproliferative Disorders +   
IMMUNOSKELETAL DYSPLASIA WITH NEURODEVELOPMENTAL ABNORMALITIES  
INFLAMMATORY BOWEL DISEASE, IMMUNODEFICIENCY, AND ENCEPHALOPATHY  
intrahepatic cholestasis +   
Liver Abscess +   
liver carcinoma in situ 
liver cirrhosis +   
Liver Fibrocystic Disease and Polydactyly 
liver inflammatory pseudotumor 
Liver Injury +   
Liver Neoplasms +   
lymphatic system disease +   
Lymphoblastic Transformation, Inhibition of 
membranoproliferative glomerulonephritis +   
mitochondrial DNA depletion syndrome 6  
Monocyte Chemotactic Disorder 
opisthorchiasis  
otulipenia  
paragonimiasis 
Parasitic Liver Diseases +   
peliosis hepatis  
Phosphoenolpyruvate Carboxykinase Deficiency +   
polycystic echinococcosis 
polycystic liver disease +   
portal hypertension +   
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. (OMIM)
Radiation Sensitivity of Natural Killer Activity 
Recurrent Infections, with Encephalopathy, Hepatic Dysfunction, and Cardiovascular Malformations  
renal-hepatic-pancreatic dysplasia +   
Retinohepatoendocrinologic Syndrome 
Thrombocytopenic Purpura +   
toxocariasis +   
Transfusion Reaction  
Transplant Rejection +   
Trichohepatoneurodevelopmental Syndrome  
tyrosinemia type II  
visceral leishmaniasis  
Wilson disease +   
Zellweger syndrome +   

Synonyms
Exact Synonyms: PTORCH2
Primary IDs: OMIM:617397
Alternate IDs: RDO:9001724

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RGD is funded by grant HL64541 from the National Heart, Lung, and Blood Institute on behalf of the NIH.