Showing entry for Congenital unilateral absence

General Disease Information
BXGD Id	BXGD006910
Disease Name	Congenital unilateral absence
Disease CUI Id	C0332909
MeSH Codes
Disease Class Name
Semantic Type	Congenital Abnormality
Human Phenotype Ontology Id
Human Phenotype Ontology Term
Disease Ontology Id
Disease Ontology Class Name
Disorder Network	disorder-protein-compound-food associations