Showing entry for Dystrophia myotonica 2

General Disease Information
BXGD Id	BXGD018049
Disease Name	Dystrophia myotonica 2
Disease CUI Id	C2931689
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
Human Phenotype Ontology Term
Disease Ontology Id	DOID:7
Disease Ontology Class Name	disease of anatomical entity
Disorder Network	disorder-protein-compound-food associations