Showing entry for Dysgenesis of the hippocampus



                               
General Disease Information
BXGD IdBXGD022835
Disease NameDysgenesis of the hippocampus
Disease CUI IdC4476591
MeSH Codes   
Disease Class Name
Semantic TypeCongenital Abnormality
Human Phenotype Ontology Id HP:0000707  
Human Phenotype Ontology TermAbnormality of the nervous system
Disease Ontology Id   
Disease Ontology Class Name
Disorder Network disorder-protein-compound-food associations