Showing entry for Hydrops Fetalis



                               
General Disease Information
BXGD IdBXGD001374
Disease NameHydrops Fetalis
Disease CUI IdC0020305
MeSH Codes C23   C16   C13   C20   C15  
Disease Class NamePathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Female Urogenital Diseases and Pregnancy Complications; Immune System Diseases; Hemic and Lymphatic Diseases
Semantic TypeDisease or Syndrome
Human Phenotype Ontology Id HP:0001939   HP:0001197  
Human Phenotype Ontology TermAbnormality of metabolism/homeostasis; Abnormality of prenatal development or birth
Disease Ontology Id   
Disease Ontology Class Name
Disorder Network disorder-protein-compound-food associations