Showing entry for Platelet aggregation abnormal



                               
General Disease Information
BXGD IdBXGD009260
Disease NamePlatelet aggregation abnormal
Disease CUI IdC0541767
MeSH Codes C16   C15  
Disease Class NameCongenital, Hereditary, and Neonatal Diseases and Abnormalities; Hemic and Lymphatic Diseases
Semantic TypeFinding
Human Phenotype Ontology Id HP:0001871  
Human Phenotype Ontology TermAbnormality of blood and blood-forming tissues
Disease Ontology Id   
Disease Ontology Class Name
Disorder Network disorder-protein-compound-food associations