Showing entry for Apert-Crouzon Disease

General Disease Information
BXGD Id	BXGD016171
Disease Name	Apert-Crouzon Disease
Disease CUI Id	C1863389
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:7
Disease Ontology Class Name	disease of anatomical entity
Disorder Network	disorder-protein-compound-food associations