Showing entry for Multiple skeletal anomalies

General Disease Information
BXGD Id	BXGD021564
Disease Name	Multiple skeletal anomalies
Disease CUI Id	C4025138
MeSH Codes	C16   C05
Disease Class Name	Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases
Semantic Type	Finding
Human Phenotype Ontology Id	HP:0000924
Human Phenotype Ontology Term	Abnormality of the skeletal system
Disease Ontology Id
Disease Ontology Class Name
Disorder Network	disorder-protein-compound-food associations