Showing entry for Bifid epiglottis



                               
General Disease Information
BXGD IdBXGD007287
Disease NameBifid epiglottis
Disease CUI IdC0339864
MeSH Codes C16   C08  
Disease Class NameCongenital, Hereditary, and Neonatal Diseases and Abnormalities; Respiratory Tract Diseases
Semantic TypeCongenital Abnormality
Human Phenotype Ontology Id HP:0002086  
Human Phenotype Ontology TermAbnormality of the respiratory system
Disease Ontology Id   
Disease Ontology Class Name
Disorder Network disorder-protein-compound-food associations