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Ontology Browser
Term:
Parent Terms Term With Siblings Child Terms
alpha-methylacyl-CoA racemase deficiency  
autoimmune disease of the nervous system +   
autonomic nervous system disease +   
BILIARY, RENAL, NEUROLOGIC, AND SKELETAL SYNDROME  
central nervous system disease +   
Chronobiology Disorders +   
Congenital Cataracts, Facial Dysmorphism, and Neuropathy  
congenital disorder of glycosylation It  
congenital nervous system abnormality +   
Danon disease  
diplegia of upper limb 
Gerstmann syndrome 
Glycogen Storage Disease 0, Liver  
Glycogen Storage Disease 0, Muscle  
glycogen storage disease I +   
glycogen storage disease II +   
glycogen storage disease III +   
glycogen storage disease IV +   
glycogen storage disease IX +   
glycogen storage disease V  
glycogen storage disease VI  
glycogen storage disease VII  
glycogen storage disease VIII  
Glycogen Storage Disease XI  
Glycogen Storage Disease XII  
Glycogen Storage Disease XIII  
glycogen storage disease XV  
herpes zoster +   
Infantile Multisystem Neurologic Disease with Osseous Fragility 
Infantile-Onset Multisystem Neurologic, Endocrine, and Pancreatic Disease +   
intestinal pseudo-obstruction +   
lethal congenital glycogen storage disease of heart  
LETM1-ASSOCIATED CLINICAL SPECTRUM WITH PREDOMINANT NERVOUS SYSTEM INVOLVEMENT  
Nerve Injuries +   
Nervous System Malformations +   
Nervous System Neoplasms +   
Nervous System Trauma +   
Neurocutaneous Syndromes +   
neurodegenerative disease +   
Neurologic Manifestations +   
Norrie disease  
peripheral nervous system disease +   
Polyglucosan Body Disease, Adult Form  
Polyglucosan Body Myopathy 1 with or without Immunodeficiency  
Polyglucosan Body Myopathy 2  
Roy Maroteaux Kremp Syndrome 
sensory system disease +   
Tang Hsi Ryu Syndrome 
toxic encephalopathy +   

Synonyms
Exact Synonyms: APBD ;   APBN ;   Adult Polyglucosan Body Disease ;   POLYGLUCOSAN BODY NEUROPATHY, ADULT FORM ;   adult polyglucosan body neuropathy
Broad Synonyms: GBE1-RELATED DISORDERS ;   GBE1-related disorder
Primary IDs: MESH:C564878
Alternate IDs: MIM:263570
Xrefs: MONDO:0009897

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