Showing entry for Congenital meningocele



                               
General Disease Information
BXGD IdBXGD011854
Disease NameCongenital meningocele
Disease CUI IdC1261470
MeSH Codes C23   C16   C10  
Disease Class NamePathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases
Semantic TypeCongenital Abnormality
Human Phenotype Ontology Id   
Human Phenotype Ontology Term
Disease Ontology Id DOID:0080015  
Disease Ontology Class Namephysical disorder
Disorder Network disorder-protein-compound-food associations