Showing entry for Epidermolysis Bullosa Dystrophica



                               
General Disease Information
BXGD IdBXGD003070
Disease NameEpidermolysis Bullosa Dystrophica
Disease CUI IdC0079294
MeSH Codes C16   C17  
Disease Class NameCongenital, Hereditary, and Neonatal Diseases and Abnormalities; Skin and Connective Tissue Diseases
Semantic TypeDisease or Syndrome
Human Phenotype Ontology Id   
Human Phenotype Ontology Term
Disease Ontology Id DOID:630   DOID:7  
Disease Ontology Class Namegenetic disease; disease of anatomical entity
Disorder Network disorder-protein-compound-food associations