Showing entry for Deficiency of prolidase

General Disease Information
BXGD Id	BXGD005974
Disease Name	Deficiency of prolidase
Disease CUI Id	C0268532
MeSH Codes	C16
Disease Class Name	Congenital, Hereditary, and Neonatal Diseases and Abnormalities
Semantic Type	Disease or Syndrome
Human Phenotype Ontology Id
Human Phenotype Ontology Term
Disease Ontology Id
Disease Ontology Class Name
Disorder Network	disorder-protein-compound-food associations