Showing entry for Congenital absence of vas deferens

General Disease Information
BXGD Id	BXGD005669
Disease Name	Congenital absence of vas deferens
Disease CUI Id	C0266444
MeSH Codes
Disease Class Name
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