Showing entry for Congenital phimosis

General Disease Information
BXGD Id	BXGD007727
Disease Name	Congenital phimosis
Disease CUI Id	C0345326
MeSH Codes	C16   C17   C12
Disease Class Name	Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Skin and Connective Tissue Diseases; Male Urogenital Diseases
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