Showing entry for Embryopathies



                               
General Disease Information
BXGD IdBXGD000872
Disease NameEmbryopathies
Disease CUI IdC0013949
MeSH Codes C16   C13  
Disease Class NameCongenital, Hereditary, and Neonatal Diseases and Abnormalities; Female Urogenital Diseases and Pregnancy Complications
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