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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 +   
Disruptions of the rhythmic cycle of bodily functions or activities.
Congenital Cataracts, Facial Dysmorphism, and Neuropathy  
congenital nervous system abnormality +   
diplegia of upper limb 
Gerstmann syndrome 
herpes zoster +   
Infantile Multisystem Neurologic Disease with Osseous Fragility 
Infantile-Onset Multisystem Neurologic, Endocrine, and Pancreatic Disease +   
intestinal pseudo-obstruction +   
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  
Roy Maroteaux Kremp Syndrome 
sensory system disease +   
Tang Hsi Ryu Syndrome 
toxic encephalopathy +   

Synonyms
Exact Synonyms: Biological Clock Disturbance ;   Biological Clock Disturbances ;   Chronobiology Disorder ;   Circadian Dysregulation ;   Circadian Rhythm Disorder ;   Circadian Rhythm Disorders ;   Psychogenic Inversion of Circadian Rhythm
Primary IDs: MESH:D021081 ;   RDO:0007327
Definition Sources: MESH:D021081

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