Showing entry for Camurati-Engelmann Syndrome

General Disease Information
BXGD Id	BXGD000765
Disease Name	Camurati-Engelmann Syndrome
Disease CUI Id	C0011989
MeSH Codes	C16   C05
Disease Class Name	Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases
Semantic Type	Disease or Syndrome
Human Phenotype Ontology Id
Human Phenotype Ontology Term
Disease Ontology Id	DOID:630   DOID:7
Disease Ontology Class Name	genetic disease; disease of anatomical entity
Disorder Network	disorder-protein-compound-food associations