Ontology Browser

Term:
PSEUDO-TORCH SYNDROME 2 (DOID:9001536)
Annotations: Rat: (1) Mouse: (1) Human: (1) Chinchilla: (1) Bonobo: (1) Dog: (1) Squirrel: (1)
Parent Terms Term With Siblings Child Terms
brain disease +     
liver disease +     
Acute Febrile Encephalopathy 
akinetic mutism 
Alcoholic Liver Diseases +   
alpha 1-antitrypsin deficiency  
alveolar echinococcosis 
amblyopia +   
Autoimmune Diseases +   
basal ganglia disease +   
baylisascariasis 
Beta-Ureidopropionase Deficiency  
Brain Abscess +   
brain compression  
Brain Death  
brain edema +   
Brain Hypoxia +   
Brain Injuries +   
Brain Neoplasms +   
Budd-Chiari syndrome +   
capillariasis 
Carnitine Palmitoyltransferase II Deficiency, Infantile  
Central Auditory Diseases +   
central nervous system origin vertigo 
cerebellar disease +   
cerebral degeneration +   
cerebritis 
cerebrovascular disease +   
Chemical and Drug Induced Liver Injury +   
Chondroitin-6-Sulfaturia, Defective Cellular Immunity, Nephrotic Syndrome 
chromosome 1p32-p31 deletion syndrome  
Chronic Brain Damage +   
clonorchiasis  
COACH Syndrome  
Colpocephaly  
complex cortical dysplasia with other brain malformations +   
Crome Syndrome 
Cyanosis and Hepatic Disease 
cystic echinococcosis 
dementia +   
Dermatoleukodystrophy 
diabetic encephalopathy  
disease of mental health +   
encephalitis +   
encephalomalacia +   
ENCEPHALOPATHY DUE TO DEFECTIVE MITOCHONDRIAL AND PEROXISOMAL FISSION 2  
ENCEPHALOPATHY, ACUTE, INFECTION-INDUCED (HERPES-SPECIFIC), 8  
ENCEPHALOPATHY, ACUTE, INFECTION-INDUCED, SUSCEPTIBILITY TO, 3  
ENCEPHALOPATHY, NEONATAL SEVERE, WITH LACTIC ACIDOSIS AND BRAIN ABNORMALITIES  
ENCEPHALOPATHY, PROGRESSIVE, EARLY-ONSET, WITH BRAIN ATROPHY AND SPASTICITY  
ENCEPHALOPATHY, PROGRESSIVE, EARLY-ONSET, WITH BRAIN ATROPHY AND THIN CORPUS CALLOSUM  
epilepsy +   
fatty liver disease +   
fetal erythroblastosis +   
Focal Nodular Hyperplasia 
Glycogen Storage Disease 0, Liver  
Graft vs Host Disease  
Granulomas, Congenital Cerebral 
GROWTH RETARDATION, INTELLECTUAL DEVELOPMENTAL DISORDER, HYPOTONIA, AND HEPATOPATHY  
GSD IV, Nonprogressive Hepatic 
Headache Disorders +   
hepatic encephalopathy +   
Hepatic Insufficiency +   
Hepatic Porphyrias +   
hepatic tuberculosis 
hepatic vascular disease +   
hepatitis +   
Hepatomegaly +   
hepatopulmonary syndrome  
hepatorenal syndrome  
heterophyiasis 
hydrocephalus +   
hypersensitivity reaction disease +   
hypoglycemic coma 
hypothalamic 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  
intracranial hypertension +   
intracranial hypotension 
intrahepatic cholestasis +   
Keratosis Follicularis Dwarfism Cerebral Atrophy 
Kuzniecky Andermann Syndrome 
Leukoencephalopathies +   
Liver Abscess +   
liver benign neoplasm +   
liver cancer +   
liver carcinoma in situ 
liver cirrhosis +   
Liver Fibrocystic Disease and Polydactyly 
liver inflammatory pseudotumor 
Liver Injury +   
lymphatic system disease +   
Lymphoblastic Transformation, Inhibition of 
lymphocytic choriomeningitis  
membranoproliferative glomerulonephritis +   
Metabolic Brain Diseases +   
mitochondrial DNA depletion syndrome 6  
Monocyte Chemotactic Disorder 
movement disease +   
NEURODEVELOPMENTAL DISORDER WITH OR WITHOUT ANOMALIES OF THE BRAIN, EYE, OR HEART  
neuroschistosomiasis 
Neutrophil Chemotactic Response, Abnormal 
Non-Lissencephalic Cortical Dysplasia 
olfactory nerve disease +   
opisthorchiasis  
otulipenia  
paragonimiasis 
Parasitic Liver Diseases +   
peliosis hepatis  
phaeohyphomycosis +  
Phosphoenolpyruvate Carboxykinase Deficiency +   
polycystic echinococcosis 
polycystic liver disease +   
porencephaly +   
portal hypertension +   
Postnatal Progressive Microcephaly with Seizures and Brain Atrophy  
primary immunodeficiency disease +   
prion disease +   
Progressive Early-Onset Encephalopathy with Episodic Rhabdomyolysis  
Progressive Encephalopathy with Amyotrophy and Optic Atrophy  
Progressive Encephalopathy, with or without Lipodystrophy  
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)
pseudobulbar palsy +  
Radiation Sensitivity of Natural Killer Activity 
Rajab Syndrome  
Rambaud Galian Syndrome 
Recurrent Infections, with Encephalopathy, Hepatic Dysfunction, and Cardiovascular Malformations  
renal-hepatic-pancreatic dysplasia +   
Retinohepatoendocrinologic Syndrome 
Sener Syndrome 
senile degeneration of brain 
Sepsis-Associated Encephalopathy  
sparganosis 
Spastic Pseudosclerosis 
Subdural Effusion 
tertiary neurosyphilis +  
thalamic disease +   
Thrombocytopenic Purpura +   
Thyrocerebral-Retinal Syndrome 
toxocariasis +   
Transfusion Reaction  
transient global amnesia 
Transplant Rejection +   
Trichohepatoneurodevelopmental Syndrome  
tyrosinemia type II  
visceral leishmaniasis  
Wernicke encephalopathy  
Wilson disease +   
Zellweger syndrome +   

Synonyms
Exact Synonyms: PTORCH2
Primary IDs: OMIM:617397 ;   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.