Showing entry for Aplasia/Hypoplasia of the corpus callosum

General Disease Information
BXGD Id	BXGD016087
Disease Name	Aplasia/Hypoplasia of the corpus callosum
Disease CUI Id	C1861866
MeSH Codes
Disease Class Name
Semantic Type	Finding
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