Showing entry for MYOFIBROMATOSIS, INFANTILE, 2

General Disease Information
BXGD Id	BXGD019571
Disease Name	MYOFIBROMATOSIS, INFANTILE, 2
Disease CUI Id	C3809084
MeSH Codes
Disease Class Name
Semantic Type	Disease or Syndrome
Human Phenotype Ontology Id
Human Phenotype Ontology Term
Disease Ontology Id	DOID:7   DOID:14566
Disease Ontology Class Name	disease of anatomical entity; disease of cellular proliferation
Disorder Network	disorder-protein-compound-food associations