Showing entry for Congenital cerebral hernia

General Disease Information
BXGD Id	BXGD000884
Disease Name	Congenital cerebral hernia
Disease CUI Id	C0014065
MeSH Codes	C23   C16   C10
Disease Class Name	Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases
Semantic Type	Congenital Abnormality
Human Phenotype Ontology Id	HP:0000152   HP:0000924
Human Phenotype Ontology Term	Abnormality of head or neck; Abnormality of the skeletal system
Disease Ontology Id
Disease Ontology Class Name
Disorder Network	disorder-protein-compound-food associations