Showing entry for FIBROMATOSIS, GINGIVAL, 2



                               
General Disease Information
BXGD IdBXGD015387
Disease NameFIBROMATOSIS, GINGIVAL, 2
Disease CUI IdC1854181
MeSH Codes C16   C07  
Disease Class NameCongenital, Hereditary, and Neonatal Diseases and Abnormalities; Stomatognathic Diseases
Semantic TypeDisease or Syndrome
Human Phenotype Ontology Id   
Human Phenotype Ontology Term
Disease Ontology Id DOID:7  
Disease Ontology Class Namedisease of anatomical entity
Disorder Network disorder-protein-compound-food associations