Showing entry for Oculomotor apraxia



                               
General Disease Information
BXGD IdBXGD018945
Disease NameOculomotor apraxia
Disease CUI IdC3489733
MeSH Codes C23   C11   C10   F01   C14  
Disease Class NamePathological Conditions, Signs and Symptoms; Eye Diseases; Nervous System Diseases; Behavior and Behavior Mechanisms; Cardiovascular Diseases
Semantic TypeDisease or Syndrome
Human Phenotype Ontology Id HP:0000707   HP:0000478  
Human Phenotype Ontology TermAbnormality of the nervous system; Abnormality of the eye
Disease Ontology Id   
Disease Ontology Class Name
Disorder Network disorder-protein-compound-food associations