Showing entry for Arnold-Chiari Malformation, Type I

General Disease Information
BXGD Id	BXGD010256
Disease Name	Arnold-Chiari Malformation, Type I
Disease CUI Id	C0750929
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