Showing entry for Congenital neurologic anomalies

General Disease Information
BXGD Id	BXGD009067
Disease Name	Congenital neurologic anomalies
Disease CUI Id	C0497552
MeSH Codes	C16   C10
Disease Class Name	Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases
Semantic Type	Congenital Abnormality
Human Phenotype Ontology Id	HP:0000707
Human Phenotype Ontology Term	Abnormality of the nervous system
Disease Ontology Id
Disease Ontology Class Name
Disorder Network	disorder-protein-compound-food associations