Showing entry for Erythroblastosis, Fetal



                               
General Disease Information
BXGD IdBXGD000947
Disease NameErythroblastosis, Fetal
Disease CUI IdC0014761
MeSH Codes C16   C13   C20   C15  
Disease Class NameCongenital, 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   
Human Phenotype Ontology Term
Disease Ontology Id DOID:7  
Disease Ontology Class Namedisease of anatomical entity
Disorder Network disorder-protein-compound-food associations