Showing entry for Accessory spleen



                               
General Disease Information
BXGD IdBXGD005703
Disease NameAccessory spleen
Disease CUI IdC0266631
MeSH Codes C16   C15  
Disease Class NameCongenital, Hereditary, and Neonatal Diseases and Abnormalities; Hemic and Lymphatic Diseases
Semantic TypeCongenital Abnormality
Human Phenotype Ontology Id HP:0025031   HP:0002715   HP:0001626  
Human Phenotype Ontology TermAbnormality of the digestive system; Abnormality of the immune system; Abnormality of the cardiovascular system
Disease Ontology Id   
Disease Ontology Class Name
Disorder Network disorder-protein-compound-food associations