Showing entry for Inherited epidermolysis bullosa



                               
General Disease Information
BXGD IdBXGD012026
Disease NameInherited epidermolysis bullosa
Disease CUI IdC1274224
MeSH Codes C16   C17  
Disease Class NameCongenital, Hereditary, and Neonatal Diseases and Abnormalities; Skin and Connective Tissue Diseases
Semantic TypeCongenital Abnormality
Human Phenotype Ontology Id   
Human Phenotype Ontology Term
Disease Ontology Id   
Disease Ontology Class Name
Disorder Network disorder-protein-compound-food associations