Showing entry for Epidermolysis bullosa, pretibial



                               
General Disease Information
BXGD IdBXGD008775
Disease NameEpidermolysis bullosa, pretibial
Disease CUI IdC0432321
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 HP:0001574  
Human Phenotype Ontology TermAbnormality of the integument
Disease Ontology Id   
Disease Ontology Class Name
Disorder Network disorder-protein-compound-food associations