Showing entry for Fibrous Hamartoma of Infancy

General Disease Information
BXGD Id	BXGD005596
Disease Name	Fibrous Hamartoma of Infancy
Disease CUI Id	C0265979
MeSH Codes	C16   C04   C17
Disease Class Name	Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Neoplasms; Skin and Connective Tissue Diseases
Semantic Type	Neoplastic Process
Human Phenotype Ontology Id	HP:0002664
Human Phenotype Ontology Term	Neoplasm
Disease Ontology Id
Disease Ontology Class Name
Disorder Network	disorder-protein-compound-food associations