Showing entry for Unilateral polymicrogyria

General Disease Information
BXGD Id	BXGD021502
Disease Name	Unilateral polymicrogyria
Disease CUI Id	C4024960
MeSH Codes	C16   C10
Disease Class Name	Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases
Semantic Type	Disease or Syndrome
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