Showing entry for Pseudopapilledema



                               
General Disease Information
BXGD IdBXGD003784
Disease NamePseudopapilledema
Disease CUI IdC0155300
MeSH Codes C16   C11   C10  
Disease Class NameCongenital, Hereditary, and Neonatal Diseases and Abnormalities; Eye Diseases; Nervous System Diseases
Semantic TypeDisease or Syndrome
Human Phenotype Ontology Id HP:0000478  
Human Phenotype Ontology TermAbnormality of the eye
Disease Ontology Id DOID:7  
Disease Ontology Class Namedisease of anatomical entity
Disorder Network disorder-protein-compound-food associations