Showing entry for 47, XYY syndrome



                               
General Disease Information
BXGD IdBXGD018604
Disease Name47, XYY syndrome
Disease CUI IdC3266843
MeSH Codes C23   C16  
Disease Class NamePathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities
Semantic TypeDisease or Syndrome
Human Phenotype Ontology Id   
Human Phenotype Ontology Term
Disease Ontology Id   
Disease Ontology Class Name
Disorder Network disorder-protein-compound-food associations