Showing entry for Fibromatosis, Gingival



                               
General Disease Information
BXGD IdBXGD001039
Disease NameFibromatosis, Gingival
Disease CUI IdC0016049
MeSH Codes C16   C07  
Disease Class NameCongenital, Hereditary, and Neonatal Diseases and Abnormalities; Stomatognathic Diseases
Semantic TypeAnatomical Abnormality
Human Phenotype Ontology Id HP:0002664   HP:0000152  
Human Phenotype Ontology TermNeoplasm; Abnormality of head or neck
Disease Ontology Id DOID:7  
Disease Ontology Class Namedisease of anatomical entity
Disorder Network disorder-protein-compound-food associations