Showing entry for Limb-girdle muscular dystrophy type 2H

General Disease Information
BXGD Id	BXGD006143
Disease Name	Limb-girdle muscular dystrophy type 2H
Disease CUI Id	C0270968
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; Congenital Abnormality
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