Showing entry for Congenital hypoplasia of penis

General Disease Information
BXGD Id	BXGD005668
Disease Name	Congenital hypoplasia of penis
Disease CUI Id	C0266435
MeSH Codes	C16
Disease Class Name	Congenital, Hereditary, and Neonatal Diseases and Abnormalities
Semantic Type	Congenital Abnormality
Human Phenotype Ontology Id	HP:0000119
Human Phenotype Ontology Term	Abnormality of the genitourinary system
Disease Ontology Id
Disease Ontology Class Name
Disorder Network	disorder-protein-compound-food associations