Send us a Message
Submit Data |  Help |  Video Tutorials |  News |  Publications |  Download |  REST API |  Citing RGD |  Contact   
Search RGD Grant Resources Citing RGD About Us Contact Us
Genes Variants Community Projects QTLs Strains Markers Genome Information Ontologies Cell Lines References Download Submit Data
OntoMate (Literature Search) JBrowse (Genome Browser) Synteny Browser (VCMap) Variant Visualizer Multi-Ontology Enrichment (MOET) Gene-Ortholog Location Finder (GOLF) InterViewer (Protein-Protein Interactions) PhenoMiner (Quatitative Phenotypes) Gene Annotator OLGA (Gene List Generator) AllianceMine GViewer (Genome Viewer)
Aging & Age-Related Disease Behavioral & Substance Use Disorder Cancer & Neoplastic Disease Cardiovascular Disease Coronavirus Disease Developmental Disease Diabetes Hematologic Disease Immune & Inflammatory Disease Infectious Disease Liver Disease Neurological Disease Obesity & Metabolic Syndrome Renal Disease Respiratory Disease Sensory Organ Disease
Find Models Genetic Models Autism Models Rat PhenoMiner (Quantitative Phenotypes) Chinchilla PhenoMiner Expected Ranges (Quantitative Phenotype) PhenoMiner Term Comparison Hybrid Rat Diversity Panel Phenotypes Phenotypes in Other Animal Models Animal Husbandry Strain Medical Records Phylogenetics Strain Availability Calendar Rats 101 Submissions Photo Archive
Pathways
Rat Community Forum Directory of Rat Laboratories Video Tutorials News RGD Publications RGD Presentations Archive Nomenclature Guidelines Resource Links Laboratory Resources Employment Resources
Advanced Search (OLGA)

Ontology Browser
Term:
Parent Terms Term With Siblings Child Terms
Axonal Encephalopathy with Necrotizing Myopathy, Cardiomyopathy, and Cataracts 
Boylan Dew Greco Syndrome 
CAMFAK Syndrome 
central pontine myelinolysis  
Demyelinating Autoimmune Diseases, CNS +   
Encephalopathy with Intracranial Calcification, Growth Hormone Deficiency, Microcephaly, and Retinal Degeneration 
Ethanolaminosis 
glutaric acidemia I  
Groll Hirschowitz Syndrome 
Hamano Tsukamoto Syndrome 
hepatic encephalopathy +   
Hereditary Central Nervous System Demyelinating Diseases +   
Hypotonia, Congenital Nystagmus, Ataxia and Abnormal Auditory Brainstem Response 
INFLAMMATORY BOWEL DISEASE, IMMUNODEFICIENCY, AND ENCEPHALOPATHY  
kernicterus +   
Marchiafava-Bignami Disease 
A neurodegenerative condition that is characterized by demyelination or necrosis of the CORPUS CALLOSUM. Symptoms include DEPRESSION; PARANOIA; DEMENTIA; SEIZURES; and ATAXIA which can progress to COMA and death in a few months. Marchiafava-Bignami syndrome is seen often in alcoholics but has been found in non-alcoholics as well.
Metabolic Brain Diseases, Inborn +   
mitochondrial encephalomyopathy +   
Ophthalmoplegic Migraine 
polyradiculoneuropathy +   
progressive multifocal leukoencephalopathy  
pyridoxamine 5'-phosphate oxidase deficiency  
Reye syndrome  
Schofer-Beetz-Bohl Syndrome 
Subacute Combined Degeneration  
TANGO2-related metabolic encephalopathy and arrythmias  
Thiamine Metabolism Dysfunction Syndrome 5 (Episodic Encephalopathy Type)  
Wernicke encephalopathy  

Synonyms
Exact Synonyms: Marchiafava-Bignami syndrome
Xrefs: EFO:1001809;  MESH:D054319;  MONDO:0016370
Definition Sources: MESH:D054319

paths to the root