Showing entry for Radioulnar Synostosis

General Disease Information
BXGD Id	BXGD003905
Disease Name	Radioulnar Synostosis
Disease CUI Id	C0158761
MeSH Codes	C16   C05
Disease Class Name	Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases
Semantic Type	Congenital Abnormality
Human Phenotype Ontology Id	HP:0040064   HP:0000924
Human Phenotype Ontology Term	Abnormality of limbs; Abnormality of the skeletal system
Disease Ontology Id	DOID:630   DOID:7   DOID:0080015
Disease Ontology Class Name	genetic disease; disease of anatomical entity; physical disorder
Disorder Network	disorder-protein-compound-food associations