Showing entry for Amelogenesis imperfecta local hypoplastic form



                               
General Disease Information
BXGD IdBXGD008238
Disease NameAmelogenesis imperfecta local hypoplastic form
Disease CUI IdC0399367
MeSH Codes C16   C07  
Disease Class NameCongenital, Hereditary, and Neonatal Diseases and Abnormalities; Stomatognathic Diseases
Semantic TypeCongenital Abnormality
Human Phenotype Ontology Id   
Human Phenotype Ontology Term
Disease Ontology Id   
Disease Ontology Class Name
Disorder Network disorder-protein-compound-food associations