Showing entry for Congenital hemihypertrophy

General Disease Information
BXGD Id	BXGD006909
Disease Name	Congenital hemihypertrophy
Disease CUI Id	C0332890
MeSH Codes	C23   C16   C13
Disease Class Name	Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Female Urogenital Diseases and Pregnancy Complications
Semantic Type	Congenital Abnormality
Human Phenotype Ontology Id	HP:0040064   HP:0001507
Human Phenotype Ontology Term	Abnormality of limbs; Growth abnormality
Disease Ontology Id
Disease Ontology Class Name
Disorder Network	disorder-protein-compound-food associations