Showing entry for Congenital microcephaly

General Disease Information
BXGD Id	BXGD017366
Disease Name	Congenital microcephaly
Disease CUI Id	C2677180
MeSH Codes	C16   C05   C10
Disease Class Name	Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases; Nervous System Diseases
Semantic Type	Congenital Abnormality
Human Phenotype Ontology Id	HP:0000707   HP:0000152   HP:0000924
Human Phenotype Ontology Term	Abnormality of the nervous system; Abnormality of head or neck; Abnormality of the skeletal system
Disease Ontology Id
Disease Ontology Class Name
Disorder Network	disorder-protein-compound-food associations