Showing entry for Scapuloperoneal myopathy

General Disease Information
BXGD Id	BXGD017993
Disease Name	Scapuloperoneal myopathy
Disease CUI Id	C2931268
MeSH Codes	C16   C05   C10
Disease Class Name	Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases; Nervous System Diseases
Semantic Type	Disease or Syndrome
Human Phenotype Ontology Id	HP:0040064   HP:0003011
Human Phenotype Ontology Term	Abnormality of limbs; Abnormality of the musculature
Disease Ontology Id	DOID:7
Disease Ontology Class Name	disease of anatomical entity
Disorder Network	disorder-protein-compound-food associations