Showing entry for Autosomal dominant epidermolysis bullosa simplex

General Disease Information
BXGD Id	BXGD005919
Disease Name	Autosomal dominant epidermolysis bullosa simplex
Disease CUI Id	C0268375
MeSH Codes	C16   C17
Disease Class Name	Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Skin and Connective Tissue Diseases
Semantic Type	Disease or Syndrome
Human Phenotype Ontology Id
Human Phenotype Ontology Term
Disease Ontology Id
Disease Ontology Class Name
Disorder Network	disorder-protein-compound-food associations